Variant report
Variant | rs61803111 |
---|---|
Chromosome Location | chr1:153372890-153372891 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:87)
- CpG islands (count:0)
- Chromatin interactive region (count:10)
- LncRNA region (count:0)
- 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 | MAZ | chr1:153372804-153373112 | K562 | blood: | n/a | n/a |
2 | JUND | chr1:153372882-153373011 | K562 | blood: | n/a | n/a |
3 | RCOR1 | chr1:153372844-153373060 | K562 | blood: | n/a | n/a |
4 | CTCF | chr1:153372889-153373045 | Hela-S3 | cervix: | n/a | n/a |
5 | CTCF | chr1:153372840-153372990 | SAEC | small airway: | n/a | n/a |
6 | CTCF | chr1:153372787-153373150 | K562 | blood: | n/a | n/a |
7 | CTCF | chr1:153372860-153373010 | BJ | skin: | n/a | n/a |
8 | RAD21 | chr1:153372842-153373045 | SK-N-SH_RA | brain: | n/a | n/a |
9 | CTCF | chr1:153372881-153373018 | MCF-7 | breast: | n/a | n/a |
10 | CTCF | chr1:153372840-153372990 | HPF | lung: | n/a | n/a |
11 | RAD21 | chr1:153372859-153373093 | SK-N-SH_RA | brain: | n/a | n/a |
12 | CTCF | chr1:153372855-153373035 | SK-N-SH_RA | brain: | n/a | n/a |
13 | RAD21 | chr1:153372844-153373049 | K562 | blood: | n/a | n/a |
14 | CTCF | chr1:153372844-153373089 | HepG2 | liver: | n/a | n/a |
15 | CTCF | chr1:153372792-153373053 | K562 | blood: | n/a | n/a |
16 | CTCF | chr1:153372860-153373010 | GM12864 | blood: | n/a | n/a |
17 | SMC3 | chr1:153372822-153373070 | Hela-S3 | cervix: | n/a | n/a |
18 | CTCF | chr1:153372860-153373010 | HBMEC | blood vessel: | n/a | n/a |
19 | RAD21 | chr1:153372847-153373150 | Hela-S3 | cervix: | n/a | n/a |
20 | CTCF | chr1:153372890-153373038 | GM19238 | blood: | n/a | n/a |
21 | CTCF | chr1:153372840-153372990 | HRPEpiC | eye: | n/a | n/a |
22 | RAD21 | chr1:153372743-153373249 | A549 | lung: | n/a | n/a |
23 | CTCF | chr1:153372879-153373064 | MCF-7 | breast: | n/a | n/a |
24 | CTCF | chr1:153372860-153373010 | AG04449 | skin: | n/a | n/a |
25 | CTCF | chr1:153372854-153373077 | K562 | blood: | n/a | n/a |
26 | CTCF | chr1:153372750-153373092 | K562 | blood: | n/a | n/a |
27 | CTCF | chr1:153372853-153373039 | MCF-7 | breast: | n/a | n/a |
28 | CTCF | chr1:153372820-153372970 | GM12874 | blood: | n/a | n/a |
29 | RAD21 | chr1:153372845-153373047 | GM12878 | blood: | n/a | n/a |
30 | CTCF | chr1:153372880-153373030 | AoAF | blood vessel: | n/a | n/a |
31 | CTCF | chr1:153372780-153372930 | A549 | lung: | n/a | n/a |
32 | CTCF | chr1:153372868-153373052 | NHEK | skin: | n/a | n/a |
33 | CTCF | chr1:153372860-153373010 | GM12865 | blood: | n/a | n/a |
34 | RAD21 | chr1:153372874-153373131 | IMR90 | lung: | n/a | n/a |
35 | CTCF | chr1:153372780-153372930 | AG04450 | lung: | n/a | n/a |
36 | CTCF | chr1:153372775-153373176 | MCF-7 | breast: | n/a | n/a |
37 | CTCF | chr1:153372880-153373030 | SK-N-SH_RA | brain: | n/a | n/a |
38 | CTCF | chr1:153372874-153373018 | MCF-7 | breast: | n/a | n/a |
39 | EBF1 | chr1:153372777-153373090 | GM12878 | blood: | n/a | chr1:153372923-153372932 chr1:153372923-153372932 chr1:153372922-153372933 chr1:153372922-153372932 chr1:153372921-153372934 |
40 | RAD21 | chr1:153372798-153373258 | HCT-116 | colon: | n/a | n/a |
41 | CTCF | chr1:153372840-153372990 | BE2_C | brain: | n/a | n/a |
42 | CTCF | chr1:153372860-153373010 | HMEC | breast: | n/a | n/a |
43 | CTCF | chr1:153372890-153373035 | GM12892 | blood: | n/a | n/a |
44 | CTCF | chr1:153372840-153372990 | HFF-Myc | foreskin: | n/a | n/a |
45 | EBF1 | chr1:153372849-153373046 | GM12878 | blood: | n/a | chr1:153372923-153372932 chr1:153372923-153372932 chr1:153372922-153372933 chr1:153372922-153372932 chr1:153372921-153372934 |
46 | CTCF | chr1:153372865-153373037 | H1-hESC | embryonic stem cell: | n/a | n/a |
47 | CTCF | chr1:153372860-153373010 | HCM | heart: | n/a | n/a |
48 | SMC3 | chr1:153372821-153373123 | K562 | blood: | n/a | n/a |
49 | RAD21 | chr1:153372767-153373229 | MCF-7 | breast: | n/a | n/a |
50 | CTCF | chr1:153372827-153373065 | IMR90 | lung: | n/a | n/a |
No data |
(count:10 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:153326747..153345757-chr1:153352900..153372983,150 | MCF-7 | breast: | |
2 | chr1:153372484..153374932-chr1:153375624..153379394,3 | MCF-7 | breast: | |
3 | chr1:153371450..153373306-chr1:153462974..153465949,3 | MCF-7 | breast: | |
4 | chr1:153324857..153325877-chr1:153372541..153373354,3 | MCF-7 | breast: | |
5 | chr1:153372721..153373690-chr1:153438049..153438638,2 | MCF-7 | breast: | |
6 | chr1:153372591..153373475-chr1:153467006..153467975,2 | MCF-7 | breast: | |
7 | chr1:153327683..153328546-chr1:153372710..153373428,3 | MCF-7 | breast: | |
8 | chr1:153372472..153373407-chr1:153467323..153468103,2 | MCF-7 | breast: | |
9 | chr1:153327801..153328677-chr1:153372451..153373073,2 | MCF-7 | breast: | |
10 | chr1:153372875..153373458-chr1:153467145..153468018,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000224784 | TF binding region |
ENSG00000163220 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11205279 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11205280 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11205281 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11205282 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11205283 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11205284 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11205285 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11205286 | 0.84[ASN][1000 genomes] |
rs11205288 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11205290 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11205291 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11205292 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11205293 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11578443 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11579041 | 0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11580424 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11580467 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11580993 | 0.86[EUR][1000 genomes] |
rs11583949 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11590633 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12023124 | 0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12029448 | 0.86[EUR][1000 genomes] |
rs12035710 | 0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12040625 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12040887 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12042217 | 0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12044231 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12047833 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2148318 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2916191 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916192 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916194 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916201 | 0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916215 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916216 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916217 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916218 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916221 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2916222 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3006475 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3006476 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3006477 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs3006479 | 0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3006480 | 0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3006482 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3006483 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3006485 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3006488 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs3014807 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs3014812 | 0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs3014878 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3014879 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3014880 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3014881 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3014885 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs34944646 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3795391 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3806232 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs41264640 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4355996 | 0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4772 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4845346 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4845347 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4845541 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4845543 | 0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs57572338 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs58127527 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs58644524 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs59655855 | 0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs59678238 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs60752752 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs61803108 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs61803109 | 0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs61803110 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs61803112 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61803337 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs61803338 | 0.82[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs61803339 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs61803340 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6659104 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6673905 | 0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6680386 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6686657 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6697489 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6702735 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs73018470 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9793023 | 0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9793935 | 0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1010488 | chr1:152901263-153670972 | Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 236 gene(s) | inside rSNPs | diseases |
2 | nsv535171 | chr1:152901263-153670972 | Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 236 gene(s) | inside rSNPs | diseases |
3 | nsv533877 | chr1:152923645-153468131 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
4 | nsv1002705 | chr1:153307852-153525589 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 152 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:153367200-153374800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr1:153368200-153374600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr1:153368600-153377600 | Enhancers | Primary monocytes fromperipheralblood | blood |
4 | chr1:153371200-153374000 | Weak transcription | Primary B cells from cord blood | blood |
5 | chr1:153371600-153373000 | Enhancers | Monocytes-CD14+_RO01746 | blood |
6 | chr1:153372200-153373000 | Flanking Active TSS | Primary neutrophils fromperipheralblood | blood |