Variant report
Variant | rs10794225 |
---|---|
Chromosome Location | chr11:50257780-50257781 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:59)
- CpG islands (count:122)
- Chromatin interactive region (count:0)
- LncRNA region (count:2)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | POLR2A | chr11:50257343-50257882 | K562 | blood: | n/a | n/a |
2 | HEY1 | chr11:50257283-50258041 | K562 | blood: | n/a | chr11:50257372-50257387 |
3 | CREB1 | chr11:50257411-50258094 | K562 | blood: | n/a | chr11:50257724-50257737 |
4 | POLR2A | chr11:50257344-50257944 | K562 | blood: | n/a | n/a |
5 | POLR2A | chr11:50257397-50257987 | SK-N-SH | brain: | n/a | n/a |
6 | HCFC1 | chr11:50257575-50257898 | K562 | blood: | n/a | n/a |
7 | EGR1 | chr11:50257609-50257827 | K562 | blood: | n/a | n/a |
8 | CREB1 | chr11:50257549-50258023 | K562 | blood: | n/a | chr11:50257724-50257737 |
9 | NFYB | chr11:50257522-50257909 | K562 | blood: | n/a | chr11:50257668-50257682 chr11:50257667-50257682 chr11:50257667-50257682 |
10 | RCOR1 | chr11:50257475-50257923 | K562 | blood: | n/a | n/a |
11 | PML | chr11:50257474-50257948 | K562 | blood: | n/a | n/a |
12 | GATA2 | chr11:50257172-50257867 | SH-SY5Y | brain: | n/a | n/a |
13 | YY1 | chr11:50257449-50258228 | SK-N-SH | brain: | n/a | chr11:50257925-50257936 |
14 | POLR2A | chr11:50257290-50258099 | K562 | blood: | n/a | n/a |
15 | EGR1 | chr11:50257540-50257866 | K562 | blood: | n/a | chr11:50257600-50257610 |
16 | MAZ | chr11:50257485-50257951 | K562 | blood: | n/a | n/a |
17 | HMGN3 | chr11:50257391-50257799 | K562 | blood: | n/a | n/a |
18 | POLR2A | chr11:50257376-50258019 | K562 | blood: | n/a | n/a |
19 | UBTF | chr11:50257636-50257804 | K562 | blood: | n/a | n/a |
20 | POLR2A | chr11:50257396-50257977 | K562 | blood: | n/a | n/a |
21 | MAX | chr11:50257439-50257850 | K562 | blood: | n/a | n/a |
22 | MAX | chr11:50257310-50258002 | SK-N-SH | brain: | n/a | n/a |
23 | TAF1 | chr11:50257356-50257947 | K562 | blood: | n/a | n/a |
24 | MYC | chr11:50257417-50257987 | K562 | blood: | n/a | n/a |
25 | MXI1 | chr11:50257754-50257790 | K562 | blood: | n/a | n/a |
26 | ATF1 | chr11:50257555-50257921 | K562 | blood: | n/a | n/a |
27 | NFYA | chr11:50257563-50257911 | K562 | blood: | n/a | chr11:50257668-50257682 chr11:50257663-50257681 chr11:50257667-50257682 chr11:50257667-50257682 |
28 | TBP | chr11:50257416-50257953 | K562 | blood: | n/a | n/a |
29 | IRF1 | chr11:50257606-50257858 | K562 | blood: | n/a | n/a |
30 | POLR2A | chr11:50257752-50257863 | Hela-S3 | cervix: | n/a | n/a |
31 | POLR2A | chr11:50257398-50257886 | SK-N-SH | brain: | n/a | n/a |
32 | YY1 | chr11:50257392-50258171 | NT2-D1 | testis: | n/a | chr11:50257925-50257936 |
33 | JUND | chr11:50257422-50257919 | K562 | blood: | n/a | chr11:50257669-50257678 |
34 | POLR2A | chr11:50257163-50258013 | K562 | blood: | n/a | n/a |
35 | POLR2A | chr11:50257237-50258009 | K562 | blood: | n/a | n/a |
36 | TAF1 | chr11:50257387-50257844 | SK-N-SH | brain: | n/a | n/a |
37 | E2F6 | chr11:50257236-50257997 | K562 | blood: | n/a | chr11:50257626-50257635 chr11:50257377-50257387 chr11:50257671-50257680 |
38 | E2F6 | chr11:50257450-50257783 | K562 | blood: | n/a | chr11:50257626-50257635 chr11:50257671-50257680 |
39 | ZMIZ1 | chr11:50257630-50257894 | K562 | blood: | n/a | n/a |
40 | POLR2A | chr11:50257316-50258064 | K562 | blood: | n/a | n/a |
41 | POLR2A | chr11:50257381-50257996 | K562 | blood: | n/a | n/a |
42 | MAX | chr11:50257279-50257958 | K562 | blood: | n/a | n/a |
43 | TBL1XR1 | chr11:50257584-50257819 | K562 | blood: | n/a | n/a |
44 | MYC | chr11:50257770-50257866 | K562 | blood: | n/a | n/a |
45 | POLR2A | chr11:50257463-50257930 | K562 | blood: | n/a | n/a |
46 | YY1 | chr11:50257473-50257830 | K562 | blood: | n/a | n/a |
47 | YY1 | chr11:50257485-50257997 | K562 | blood: | n/a | chr11:50257925-50257936 |
48 | MAX | chr11:50257284-50257858 | SK-N-SH | brain: | n/a | n/a |
49 | YY1 | chr11:50257467-50258074 | SK-N-SH_RA | brain: | n/a | chr11:50257925-50257936 |
50 | ATF3 | chr11:50257564-50257818 | K562 | blood: | n/a | chr11:50257726-50257746 chr11:50257724-50257737 chr11:50257584-50257592 chr11:50257723-50257738 chr11:50257725-50257736 |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:50257752-50257802 | GM12891 | blood: | n/a |
2 | chr11:50257752-50257802 | H1-hESC | embryonic stem cell: | embryo |
3 | chr11:50257771-50257821 | GM12892 | blood: | n/a |
4 | chr11:50257771-50257821 | AG10803 | skin: | n/a |
5 | chr11:50257771-50257821 | HEK293 | kidney: | embryo |
6 | chr11:50257771-50257821 | IMR90 | lung: | fetal |
7 | chr11:50257752-50257802 | HL-60 | blood: | n/a |
8 | chr11:50257771-50257821 | HIPEpiC | eye: | n/a |
9 | chr11:50257771-50257821 | HAEpiC | amniotic membrane: | n/a |
10 | chr11:50257752-50257802 | SAEC | small airway: | n/a |
11 | chr11:50257752-50257802 | AG09319 | gingival: | n/a |
12 | chr11:50257771-50257821 | BE2_C | brain: | n/a |
13 | chr11:50257752-50257802 | T-47D | breast: | n/a |
14 | chr11:50257771-50257821 | HCT-116 | colon: | n/a |
15 | chr11:50257752-50257802 | HRE | kidney: | n/a |
16 | chr11:50257771-50257821 | CMK | blood: | n/a |
17 | chr11:50257771-50257821 | HMEC | breast: | n/a |
18 | chr11:50257771-50257821 | MCF10A-Er-Src | breast: | n/a |
19 | chr11:50257752-50257802 | SK-N-SH | brain: | n/a |
20 | chr11:50257752-50257802 | IMR90 | lung: | fetal |
21 | chr11:50257752-50257802 | HRPEpiC | eye: | n/a |
22 | chr11:50257752-50257802 | PFSK-1 | brain: | n/a |
23 | chr11:50257752-50257802 | BJ | skin: | n/a |
24 | chr11:50257752-50257802 | Hepatocyte | liver: | n/a |
25 | chr11:50257752-50257802 | CMK | blood: | n/a |
26 | chr11:50257771-50257821 | HRPEpiC | eye: | n/a |
27 | chr11:50257752-50257802 | HEK293 | kidney: | embryo |
28 | chr11:50257752-50257802 | GM06990 | blood: | n/a |
29 | chr11:50257771-50257821 | PFSK-1 | brain: | n/a |
30 | chr11:50257771-50257821 | AoSMC | blood vessel: | n/a |
31 | chr11:50257771-50257821 | SK-N-SH_RA | brain: | n/a |
32 | chr11:50257752-50257802 | RPTEC | kidney: | n/a |
33 | chr11:50257752-50257802 | NB4 | blood: | n/a |
34 | chr11:50257771-50257821 | HRCEpiC | kidney: | n/a |
35 | chr11:50257752-50257802 | NHDF-neo | bronchial: | n/a |
36 | chr11:50257771-50257821 | PrEC | prostate: | n/a |
37 | chr11:50257752-50257802 | HAEpiC | amniotic membrane: | n/a |
38 | chr11:50257771-50257821 | AG04449 | skin: | fetal |
39 | chr11:50257752-50257802 | NT2-D1 | testis: | n/a |
40 | chr11:50257752-50257802 | K562 | blood: | n/a |
41 | chr11:50257771-50257821 | HL-60 | blood: | n/a |
42 | chr11:50257771-50257821 | HRE | kidney: | n/a |
43 | chr11:50257771-50257821 | ECC-1 | luminal epithelium: | n/a |
44 | chr11:50257752-50257802 | Jurkat | blood: | n/a |
45 | chr11:50257752-50257802 | PANC-1 | pancreas: | n/a |
46 | chr11:50257752-50257802 | HNPCEpiC | eye: | n/a |
47 | chr11:50257771-50257821 | PANC-1 | pancreas: | n/a |
48 | chr11:50257752-50257802 | HCF | heart: | n/a |
49 | chr11:50257771-50257821 | SK-N-SH | brain: | n/a |
50 | chr11:50257771-50257821 | Hela-S3 | cervix: | n/a |
No data |
(count:2 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-OR4C13-1 | chr11:50257750-50258088 | ENSG00000254518 |
2 | lnc-OR4C13-1 | chr11:50257750-50258210 | NONHSAT021336 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000255042 | TF binding region |
ENSG00000254518 | TF binding region |
ENSG00000254518 | CpG island |
ENSG00000255042 | CpG island |
rs_ID | r2[population] |
---|---|
rs10794230 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs10794233 | 0.85[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs10901907 | 0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10901908 | 0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10901910 | 0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10901924 | 0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10901926 | 0.82[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs10901929 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs10901930 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs10901933 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs10901937 | 0.87[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs10901938 | 0.86[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs10902068 | 0.81[AMR][1000 genomes] |
rs1096845 | 0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11245615 | 0.83[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs11245617 | 0.80[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs11245621 | 0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11245622 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11245623 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11245625 | 0.88[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs11245645 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs11245646 | 0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs11245676 | 0.87[AMR][1000 genomes] |
rs11494317 | 0.84[AMR][1000 genomes] |
rs11518814 | 0.86[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs11523530 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs12285986 | 0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12360817 | 0.83[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs12416700 | 0.87[AMR][1000 genomes] |
rs12420462 | 0.82[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs12786030 | 0.87[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs1580562 | 0.86[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs1580563 | 0.87[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs1586631 | 0.87[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs1602128 | 0.87[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs1826089 | 0.87[AMR][1000 genomes] |
rs1844411 | 0.95[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1854691 | 0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1906893 | 0.86[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs2130308 | 0.95[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2204193 | 0.85[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs2204194 | 0.87[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs2687653 | 0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs2773516 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs2872366 | 0.82[AMR][1000 genomes] |
rs2890925 | 0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs35663418 | 0.87[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs3750371 | 0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs3861713 | 0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3904260 | 0.86[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs3904261 | 0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs3904264 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs3904271 | 0.86[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs3904273 | 0.87[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs3904275 | 0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs3905772 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs3908632 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs3908633 | 0.86[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs3912717 | 0.87[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs3912718 | 0.87[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs4065258 | 0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4065259 | 0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4065357 | 0.87[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs4065358 | 0.87[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs4065932 | 0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4065934 | 0.86[AMR][1000 genomes] |
rs4104102 | 0.85[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs4111475 | 0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4242813 | 0.90[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs4466822 | 0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4471409 | 0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4543984 | 0.87[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs4568997 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs4614442 | 0.85[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs4620713 | 0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4881639 | 0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4881678 | 0.88[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs4881684 | 0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4881685 | 0.90[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs4881686 | 0.88[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs4881690 | 0.88[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs4881711 | 0.87[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs4881714 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs4881718 | 0.85[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs4963083 | 0.87[AMR][1000 genomes] |
rs512988 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs539590 | 0.87[AMR][1000 genomes] |
rs543089 | 0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs543204 | 0.82[AMR][1000 genomes] |
rs545715 | 0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs691860 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs691973 | 0.95[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs692156 | 0.87[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs692236 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs692305 | 0.87[AMR][1000 genomes] |
rs692501 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs692557 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs692607 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs692671 | 0.87[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs7124384 | 0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7293968 | 0.87[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs7294277 | 0.95[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7483008 | 0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7932815 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs7946837 | 0.81[AMR][1000 genomes] |
rs7947751 | 0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7948363 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7949584 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs8189051 | 0.95[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs9666509 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1051021 | chr11:49692184-50658777 | ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
2 | nsv1048074 | chr11:49823455-50302232 | ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
3 | nsv1036701 | chr11:49846590-50769305 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
4 | nsv897498 | chr11:49997431-50325741 | Strong transcription ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
5 | nsv554395 | chr11:50008258-50642550 | ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
6 | nsv1047235 | chr11:50012174-50769305 | ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
7 | nsv1051699 | chr11:50013671-50769305 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
8 | nsv1037403 | chr11:50019556-50751358 | ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
9 | nsv1044792 | chr11:50019556-50769305 | ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
10 | esv2758270 | chr11:50056424-50447563 | Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
11 | esv2759827 | chr11:50056424-50449192 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
12 | nsv467877 | chr11:50057854-50642550 | Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
13 | nsv554396 | chr11:50057854-50642550 | Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
14 | esv3693389 | chr11:50058095-50713402 | Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
15 | nsv897504 | chr11:50121285-50275257 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
16 | nsv469594 | chr11:50121285-50285880 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
17 | nsv482621 | chr11:50121285-50285880 | ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
18 | nsv897505 | chr11:50121285-50292520 | Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
19 | nsv1035439 | chr11:50121285-50524009 | ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
20 | nsv1049947 | chr11:50121285-50524009 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
21 | nsv1035641 | chr11:50121285-50573214 | ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
22 | nsv1041731 | chr11:50121285-50590065 | ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
23 | nsv1053769 | chr11:50121285-50613401 | ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
24 | nsv1042046 | chr11:50121285-50637245 | ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
25 | nsv1051675 | chr11:50121285-50637245 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
26 | nsv554397 | chr11:50121285-50642550 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
27 | nsv554402 | chr11:50121285-50642550 | ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
28 | nsv897506 | chr11:50121285-50642550 | ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
29 | nsv1047502 | chr11:50121285-50651567 | Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
30 | nsv1051055 | chr11:50121285-50658777 | ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
31 | nsv554400 | chr11:50121285-50736106 | Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
32 | nsv554398 | chr11:50121285-50738763 | Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
33 | nsv554399 | chr11:50121285-50766308 | ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
34 | nsv554401 | chr11:50121285-50766308 | ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
35 | nsv1035727 | chr11:50121285-50769305 | ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
36 | nsv1036371 | chr11:50121285-50769305 | ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
37 | nsv1042993 | chr11:50121285-50769305 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
38 | nsv1045083 | chr11:50121285-50769305 | ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
39 | nsv1051800 | chr11:50121285-50769305 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
40 | nsv1051873 | chr11:50121285-50769305 | ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
41 | nsv897507 | chr11:50121285-51093950 | ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
42 | nsv1040407 | chr11:50121285-51095992 | Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
43 | esv2760366 | chr11:50138650-50524009 | Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
44 | nsv832149 | chr11:50142116-50316451 | Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
45 | nsv897508 | chr11:50152718-50304124 | Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
46 | nsv897509 | chr11:50152718-50440270 | ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
47 | nsv554403 | chr11:50164027-50766308 | ZNF genes & repeats Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
48 | esv2757444 | chr11:50171877-50449192 | ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
49 | nsv897511 | chr11:50182364-50304124 | ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
50 | nsv897512 | chr11:50185153-50258453 | Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS | TF binding regionCpG islandlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:50256200-50258600 | Active TSS | K562 | blood |
2 | chr11:50257000-50258200 | ZNF genes & repeats | Fetal Adrenal Gland | Adrenal Gland |
3 | chr11:50257200-50258000 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
4 | chr11:50257200-50258000 | ZNF genes & repeats | Gastric | stomach |
5 | chr11:50257200-50258000 | ZNF genes & repeats | Pancreas | Pancrea |
6 | chr11:50257200-50258200 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
7 | chr11:50257400-50258000 | Active TSS | Fetal Lung | lung |
8 | chr11:50257400-50258800 | ZNF genes & repeats | Placenta | Placenta |