Variant report
Variant | nsv527054 |
---|---|
Chromosome Location | chr3:556800-1350458 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:2561)
- CpG islands (count:917)
- Chromatin interactive region (count:68)
- LncRNA region (count:22)
- 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 | ATF1 | chr3:1235289-1235354 | K562 | blood: | n/a | n/a |
2 | ATF1 | chr3:1056506-1056524 | K562 | blood: | n/a | n/a |
3 | ATF2 | chr3:1172821-1173212 | H1-hESC | embryonic stem cell: | n/a | n/a |
4 | BACH1 | chr3:888492-888519 | H1-hESC | embryonic stem cell: | n/a | n/a |
5 | BACH1 | chr3:954485-954653 | H1-hESC | embryonic stem cell: | n/a | n/a |
6 | BACH1 | chr3:1135881-1135904 | H1-hESC | embryonic stem cell: | n/a | n/a |
7 | BACH1 | chr3:1249806-1249899 | H1-hESC | embryonic stem cell: | n/a | chr3:1249829-1249843 |
8 | BACH1 | chr3:577662-577951 | H1-hESC | embryonic stem cell: | n/a | n/a |
9 | BACH1 | chr3:1277576-1277666 | H1-hESC | embryonic stem cell: | n/a | n/a |
10 | BATF | chr3:954370-954767 | GM12878 | blood: | n/a | chr3:954539-954550 chr3:954567-954578 chr3:954595-954606 |
11 | BATF | chr3:599827-600084 | GM12878 | blood: | n/a | chr3:599953-599962 |
12 | BATF | chr3:954466-954707 | GM12878 | blood: | n/a | chr3:954539-954550 chr3:954567-954578 chr3:954595-954606 |
13 | BATF | chr3:638972-639242 | GM12878 | blood: | n/a | chr3:639093-639102 |
14 | BATF | chr3:892892-893121 | GM12878 | blood: | n/a | chr3:892988-892999 |
15 | BATF | chr3:599789-600089 | GM12878 | blood: | n/a | chr3:599953-599962 |
16 | BATF | chr3:892848-893082 | GM12878 | blood: | n/a | chr3:892988-892999 |
17 | BCL11A | chr3:954445-954734 | GM12878 | blood: | n/a | n/a |
18 | BCL3 | chr3:1149010-1149230 | GM12878 | blood: | n/a | n/a |
19 | BCLAF1 | chr3:599656-600200 | GM12878 | blood: | n/a | chr3:599779-599788 chr3:599826-599835 |
20 | BHLHE40 | chr3:943924-944164 | GM12878 | blood: | n/a | n/a |
21 | BHLHE40 | chr3:895419-895457 | GM12878 | blood: | n/a | n/a |
22 | BHLHE40 | chr3:846853-846863 | GM12878 | blood: | n/a | n/a |
23 | BRCA1 | chr3:817416-817453 | Hela-S3 | cervix: | n/a | n/a |
24 | BRCA1 | chr3:649451-649478 | Hela-S3 | cervix: | n/a | n/a |
25 | BRCA1 | chr3:1123741-1124044 | Hela-S3 | cervix: | n/a | n/a |
26 | BRCA1 | chr3:961437-961458 | GM12878 | blood: | n/a | n/a |
27 | BRCA1 | chr3:815996-816027 | Hela-S3 | cervix: | n/a | n/a |
28 | BRCA1 | chr3:1128644-1129340 | Hela-S3 | cervix: | n/a | n/a |
29 | BRCA1 | chr3:754720-755580 | Hela-S3 | cervix: | n/a | n/a |
30 | BRCA1 | chr3:991509-991520 | H1-hESC | embryonic stem cell: | n/a | n/a |
31 | BRCA1 | chr3:1225226-1225621 | Hela-S3 | cervix: | n/a | n/a |
32 | BRCA1 | chr3:674381-674581 | H1-hESC | embryonic stem cell: | n/a | n/a |
33 | BRCA1 | chr3:638578-639330 | Hela-S3 | cervix: | n/a | n/a |
34 | BRCA1 | chr3:639591-639851 | Hela-S3 | cervix: | n/a | n/a |
35 | CEBPB | chr3:1285013-1285370 | H1-hESC | embryonic stem cell: | n/a | chr3:1285182-1285193 |
36 | CEBPB | chr3:611097-611344 | HepG2 | liver: | n/a | chr3:611201-611212 |
37 | CEBPB | chr3:1164116-1164342 | HepG2 | liver: | n/a | chr3:1164197-1164208 |
38 | CEBPB | chr3:1128706-1129408 | Hela-S3 | cervix: | n/a | chr3:1129164-1129175 chr3:1128961-1128973 |
39 | CEBPB | chr3:766071-766268 | HepG2 | liver: | n/a | chr3:766173-766184 |
40 | CEBPB | chr3:1189136-1189409 | HepG2 | liver: | n/a | chr3:1189266-1189277 |
41 | CEBPB | chr3:650024-650224 | A549 | lung: | n/a | chr3:650073-650084 chr3:650075-650084 |
42 | CEBPB | chr3:672488-672700 | HepG2 | liver: | n/a | chr3:672554-672567 chr3:672555-672566 |
43 | CEBPB | chr3:746911-747209 | Hela-S3 | cervix: | n/a | n/a |
44 | CEBPB | chr3:1266757-1267048 | HepG2 | liver: | n/a | chr3:1266885-1266896 |
45 | CEBPB | chr3:986539-986753 | Hela-S3 | cervix: | n/a | chr3:986667-986678 |
46 | CEBPB | chr3:650039-650244 | HepG2 | liver: | n/a | chr3:650073-650084 chr3:650075-650084 |
47 | CEBPB | chr3:920402-920815 | Hela-S3 | cervix: | n/a | n/a |
48 | CEBPB | chr3:1343908-1344126 | HepG2 | liver: | n/a | chr3:1344018-1344029 chr3:1344018-1344031 |
49 | CEBPB | chr3:1224983-1225817 | Hela-S3 | cervix: | n/a | chr3:1225189-1225200 chr3:1225191-1225200 chr3:1225191-1225202 chr3:1225191-1225200 chr3:1225189-1225202 chr3:1225189-1225202 chr3:1225191-1225200 chr3:1225191-1225200 |
50 | CEBPB | chr3:591255-591764 | Hela-S3 | cervix: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:1134528-1134578 | Jurkat | blood: | n/a |
2 | chr3:1134711-1134761 | CMK | blood: | n/a |
3 | chr3:1134528-1134578 | Jurkat | blood: | n/a |
4 | chr3:1134711-1134761 | CMK | blood: | n/a |
5 | chr3:1134711-1134761 | HCT-116 | colon: | n/a |
6 | chr3:1173560-1173610 | AG09319 | gingival: | n/a |
7 | chr3:782757-782807 | ovcar-3 | ovarian: | n/a |
8 | chr3:1134528-1134578 | HL-60 | blood: | n/a |
9 | chr3:1050278-1050328 | HL-60 | blood: | n/a |
10 | chr3:782757-782807 | SK-N-SH_RA | brain: | n/a |
11 | chr3:1133865-1133915 | K562 | blood: | n/a |
12 | chr3:1284705-1284755 | Hela-S3 | cervix: | n/a |
13 | chr3:1173560-1173610 | SK-N-SH_RA | brain: | n/a |
14 | chr3:1134528-1134578 | GM12878 | blood: | n/a |
15 | chr3:1202463-1202513 | ProgFib | skin: | n/a |
16 | chr3:577821-577871 | T-47D | breast: | n/a |
17 | chr3:1173560-1173610 | RPTEC | kidney: | n/a |
18 | chr3:1050278-1050328 | SK-N-SH_RA | brain: | n/a |
19 | chr3:1134366-1134416 | PrEC | prostate: | n/a |
20 | chr3:1284705-1284755 | HCF | heart: | n/a |
21 | chr3:1134366-1134416 | GM06990 | blood: | n/a |
22 | chr3:577964-578014 | AG10803 | skin: | n/a |
23 | chr3:1133865-1133915 | BJ | skin: | n/a |
24 | chr3:1229376-1229426 | SK-N-SH | brain: | n/a |
25 | chr3:1134005-1134055 | HNPCEpiC | eye: | n/a |
26 | chr3:1134730-1134780 | ovcar-3 | ovarian: | n/a |
27 | chr3:1229376-1229426 | NB4 | blood: | n/a |
28 | chr3:1134730-1134780 | GM12892 | blood: | n/a |
29 | chr3:577821-577871 | SK-N-SH_RA | brain: | n/a |
30 | chr3:1134366-1134416 | HEK293 | kidney: | embryo |
31 | chr3:1284705-1284755 | GM19239 | blood: | n/a |
32 | chr3:1284705-1284755 | HNPCEpiC | eye: | n/a |
33 | chr3:1133865-1133915 | NHDF-neo | bronchial: | n/a |
34 | chr3:577629-577679 | MCF-7 | breast: | n/a |
35 | chr3:577964-578014 | HRPEpiC | eye: | n/a |
36 | chr3:1284705-1284755 | SK-N-SH | brain: | n/a |
37 | chr3:1173560-1173610 | SK-N-MC | brain: | n/a |
38 | chr3:577629-577679 | PFSK-1 | brain: | n/a |
39 | chr3:577629-577679 | HNPCEpiC | eye: | n/a |
40 | chr3:1202463-1202513 | AoSMC | blood vessel: | n/a |
41 | chr3:1134711-1134761 | GM12878 | blood: | n/a |
42 | chr3:1284705-1284755 | Hepatocyte | liver: | n/a |
43 | chr3:1229376-1229426 | HL-60 | blood: | n/a |
44 | chr3:1229376-1229426 | HCPEpiC | choroid plexus: | n/a |
45 | chr3:1134730-1134780 | MCF-7 | breast: | n/a |
46 | chr3:1229376-1229426 | U87 | brain: | n/a |
47 | chr3:1284705-1284755 | HRCEpiC | kidney: | n/a |
48 | chr3:577821-577871 | MCF10A-Er-Src | breast: | n/a |
49 | chr3:577821-577871 | CMK | blood: | n/a |
50 | chr3:1133865-1133915 | ECC-1 | luminal epithelium: | n/a |
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr21:9533639..9536328-chr3:614645..617390,2 | MCF-7 | breast: | |
2 | chr3:709932..711493-chr3:712317..715172,2 | K562 | blood: | |
3 | chr3:1145760..1147872-chr3:1156472..1158821,2 | K562 | blood: | |
4 | chr3:829999..831597-chr3:832456..834541,2 | MCF-7 | breast: | |
5 | chr3:805612..808013-chr3:811141..813375,2 | K562 | blood: | |
6 | chr3:950629..951227-chr3:2029405..2030169,2 | MCF-7 | breast: | |
7 | chr3:844122..846364-chr3:847958..849773,2 | K562 | blood: | |
8 | chr3:674217..674800-chr3:1123463..1123990,2 | MCF-7 | breast: | |
9 | chr3:829999..831597-chr3:832456..834541,2 | MCF-7 | breast: | |
10 | chr3:565796..568589-chr3:571178..572728,2 | K562 | blood: | |
11 | chr3:1271635..1273502-chr3:1276225..1279196,2 | K562 | blood: | |
12 | chr3:571404..573075-chr3:573790..576325,2 | MCF-7 | breast: | |
13 | chr3:565796..568589-chr3:571178..572728,2 | K562 | blood: | |
14 | chr3:746367..749271-chr3:749542..752426,2 | K562 | blood: | |
15 | chr3:703062..705164-chr3:828470..830008,2 | K562 | blood: | |
16 | chr21:9537493..9539688-chr3:612236..614804,2 | MCF-7 | breast: | |
17 | chr3:1185425..1187107-chr3:1188609..1190735,2 | K562 | blood: | |
18 | chr3:731301..733205-chr3:733252..736265,3 | K562 | blood: | |
19 | chr3:556350..557928-chr3:558208..559835,2 | MCF-7 | breast: | |
20 | chr3:674203..674975-chr3:2197712..2198482,2 | MCF-7 | breast: | |
21 | chr3:844122..846364-chr3:847958..849773,2 | K562 | blood: | |
22 | chr3:674217..674800-chr3:1123463..1123990,2 | MCF-7 | breast: | |
23 | chr3:805612..808013-chr3:811141..813375,2 | K562 | blood: | |
24 | chr12:101154422..101155178-chr3:753774..754622,2 | MCF-7 | breast: | |
25 | chr3:522873..523625-chr3:674344..674995,2 | MCF-7 | breast: | |
26 | chr2:44471645..44472524-chr3:1084585..1085105,2 | K562 | blood: | |
27 | chr3:731301..733205-chr3:733252..736265,3 | K562 | blood: | |
28 | chr12:51631069..51633376-chr3:1005382..1008189,2 | MCF-7 | breast: | |
29 | chr3:1123403..1124144-chr3:2029373..2030343,3 | MCF-7 | breast: | |
30 | chr3:554700..557337-chr3:557649..560284,2 | K562 | blood: | |
31 | chr3:1233578..1235618-chr3:1243417..1246040,2 | K562 | blood: | |
32 | chr3:762317..764340-chr3:779905..782757,2 | K562 | blood: | |
33 | chr21:9517250..9519290-chr3:632442..635070,2 | MCF-7 | breast: | |
34 | chr3:1183195..1185033-chr3:1185128..1187712,2 | MCF-7 | breast: | |
35 | chr3:1091106..1092914-chr3:1094575..1097571,2 | K562 | blood: | |
36 | chr3:1017513..1019704-chr9:130832900..130835546,2 | MCF-7 | breast: | |
37 | chr3:1089175..1092606-chr3:1092889..1096075,3 | K562 | blood: | |
38 | chr3:1091106..1092914-chr3:1094575..1097571,2 | K562 | blood: | |
39 | chr3:709932..711493-chr3:712317..715172,2 | K562 | blood: | |
40 | chr3:1271635..1274308-chr3:1276225..1277746,2 | K562 | blood: | |
41 | chr20:19743891..19744638-chr3:1326228..1327123,2 | MCF-7 | breast: | |
42 | chr3:746367..749271-chr3:749542..752426,2 | K562 | blood: | |
43 | chr3:1049665..1052589-chr3:1054165..1056315,2 | K562 | blood: | |
44 | chr3:1271635..1274308-chr3:1276225..1277746,2 | K562 | blood: | |
45 | chr3:1145760..1147872-chr3:1156472..1158821,2 | K562 | blood: | |
46 | chr17:59489294..59491290-chr3:1177376..1179707,2 | MCF-7 | breast: | |
47 | chr3:1185425..1187107-chr3:1188609..1190735,2 | K562 | blood: | |
48 | chr3:751166..753010-chr3:765105..767568,2 | K562 | blood: | |
49 | chr20:12921782..12922300-chr3:762237..762760,2 | MCF-7 | breast: | |
50 | chr3:943774..944505-chr3:1390119..1390838,2 | MCF-7 | breast: |
(count:22 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-CNTN6-2 | chr3:898848-898956 | NONHSAT087575 |
2 | lnc-CHL1-6 | chr3:608788-608866 | ucscGeneNc_uc003boy_1 |
3 | lnc-CHL1-3 | chr3:577936-578010 | ENSG00000224957 |
4 | lnc-CHL1-3 | chr3:577941-579275 | NONHSAT087570 |
5 | lnc-CHL1-3 | chr3:882398-882493 | NR_110118 |
6 | lnc-CHL1-3 | chr3:791898-791933 | NR_110118 |
7 | lnc-CHL1-3 | chr3:633788-633866 | NR_110118 |
8 | lnc-CNTN6-2 | chr3:899428-899774 | XLOC_002565 |
9 | lnc-CNTN6-1 | chr3:1051052-1054618 | XLOC_002566 |
10 | lnc-CHL1-6 | chr3:857398-857493 | ucscGeneNc_uc003boy_1 |
11 | lnc-CHL1-3 | chr3:884059-884327 | ENSG00000224957 |
12 | lnc-CNTN6-1 | chr3:1049819-1049950 | XLOC_002566 |
13 | lnc-CHL1-3 | chr3:633788-633866 | ENSG00000224957 |
14 | lnc-CHL1-6 | chr3:766898-766933 | ucscGeneNc_uc003boy_1 |
15 | lnc-CNTN6-2 | chr3:899428-900630 | NONHSAT087575 |
16 | lnc-CHL1-3 | chr3:884059-887698 | NR_110118 |
17 | lnc-IL5RA-13 | chr3:1107266-1107559 | NONHSAT087577 |
18 | lnc-CHL1-6 | chr3:859059-862698 | ucscGeneNc_uc003boy_1 |
19 | lnc-CHL1-3 | chr3:791898-791933 | ENSG00000224957 |
20 | lnc-CHL1-3 | chr3:868690-868816 | ENSG00000224957 |
21 | lnc-IL5RA-14 | chr3:659472-659997 | NONHSAT087571 |
22 | lnc-CNTN6-2 | chr3:898807-898956 | XLOC_002565 |
No data |
No data |
Variant related genes | Relation type |
---|---|
RN7SL120P | TF binding region |
CNTN6 | TF binding region |
ENSG00000235158 | TF binding region |
ENSG00000224957 | TF binding region |
ENSG00000224239 | TF binding region |
ENSG00000238075 | TF binding region |
RN7SL120P | CpG island |
CNTN6 | CpG island |
ENSG00000235158 | CpG island |
ENSG00000224957 | CpG island |
ENSG00000224239 | CpG island |
ENSG00000238075 | CpG island |
ENSG00000183283 | chromatin interactions |
ENSG00000235158 | chromatin interactions |
COPS7A | miRNA target sites |
IL10 | miRNA target sites |
HIF1A | miRNA target sites |
CPEB4 | miRNA target sites |
DCBLD2 | miRNA target sites |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs558746089 | chr3:560624-560625 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs577331141 | chr3:560658-560659 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs138192487 | chr3:560690-560691 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs541238818 | chr3:560710-560711 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs530417362 | chr3:560714-560715 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs542283036 | chr3:560792-560793 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs112982488 | chr3:560818-560819 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs9871075 | chr3:560819-560820 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
9 | rs9856277 | chr3:560824-560825 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
10 | rs186269698 | chr3:560860-560861 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs564284268 | chr3:560865-560866 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs528228331 | chr3:560920-560921 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs142198644 | chr3:560961-560962 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs145919369 | chr3:560974-560975 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs535726947 | chr3:561012-561013 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs535939539 | chr3:561017-561018 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs550186505 | chr3:561037-561038 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs117149888 | chr3:561048-561049 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs539160615 | chr3:561059-561060 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs191006996 | chr3:561089-561090 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs577370726 | chr3:561101-561102 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs557520305 | chr3:561113-561114 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs534952954 | chr3:561130-561131 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs553521456 | chr3:561153-561154 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs576184340 | chr3:561213-561214 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs148224369 | chr3:561217-561218 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs563688790 | chr3:561240-561241 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs558727070 | chr3:561252-561253 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs575669744 | chr3:561269-561270 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs373694768 | chr3:561271-561272 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs376398680 | chr3:561281-561282 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs540950477 | chr3:561324-561325 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs367977815 | chr3:561326-561327 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs564471948 | chr3:561332-561333 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs74808713 | chr3:561336-561337 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs72989702 | chr3:561368-561369 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs9860964 | chr3:561404-561405 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
38 | rs181956816 | chr3:561410-561411 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs372567874 | chr3:561450-561451 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs137954421 | chr3:561468-561469 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs538998959 | chr3:561469-561470 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs550957600 | chr3:561473-561474 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs566485024 | chr3:561494-561495 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs533868448 | chr3:561528-561529 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs553318144 | chr3:561566-561567 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs66836464 | chr3:561589-561590 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
47 | rs371210406 | chr3:561618-561619 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs77007140 | chr3:561624-561625 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
49 | rs75175508 | chr3:561641-561642 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs557642348 | chr3:561656-561657 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Cancer | 20164920 | CNVD |
Lung cancer | 16618734 | CNVD |
Autism | 18349135 | CNVD |
Breast cancer | 20409316 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Autism | 22241247 | CNVD |
Intellectual disability | 22045946 | CNVD |
Squamous cell cancer | 19607727 | CNVD |
Gastric adenocarcinoma | 19115996 | CNVD |
sporadic birth defects | 19047251 | CNVD |
Mental retardation | 17124404 | CNVD |
abnormal development | 18461090 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Sudden cardiac death | 19188705 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Acute lymphoblastic leukemia | 21339820 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Ovarian cancer | 21720365 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Papillary thyroid carcinoma | 21436994 | CNVD |
Biliary cancer | 19435499 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Esophageal squamous carcinoma | 18405350 | CNVD |
Breast cancer | 17603634 | CNVD |
Neuroblastoma | 17327916 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Colorectal cancer | 21297112 | CNVD |
Lynch syndrome | 18415027 | CNVD |
Renal cell carcinoma | 18592004 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Urothelial carcinoma | 18382360 | CNVD |
Melanoma | 18172304 | CNVD |
Cervical cancer | 21062161 | CNVD |
Hirschsprung''s Disease | 21712996 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
Insulin resistance | 16721378 | CNVD |
Neuroblastoma | 18664255 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Neuroblastoma | 21484798 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
Oral cancer | 19627613 | CNVD |
Renal cell carcinoma | 19461508 | CNVD |
Epithelial cancer | 22065749 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Liposarcoma | 21253554 | CNVD |
Basal cell lymphoma | 21115979 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Pancreatic endocrine tumor | 20981439 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 21264507 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Oral cancer | 21386901 | CNVD |
Cutaneous squamous cell carcinomas | 19131950 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Retinoblastoma | 21504564 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Breast cancer | 21364760 | CNVD |
Schizophrenia | 20967226 | CNVD |
Autism | 22543975 | CNVD |
Attention deficit hyperactivity disorder | 19546859 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Non-syndromic sensorineural hearing loss | 17289997 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Renal cell carcinoma | 21668985 | CNVD |
Tetralogy of Fallot | 22912587 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Autism | 20685689 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
early-passage human iPS cells | 21368824 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
Lung cancer | 20668451 | CNVD |
Breast cancer | 20668451 | CNVD |
Cancer | 20668451 | CNVD |
Ovarian cancer | 20668451 | CNVD |
Pancreas cancer | 20668451 | CNVD |
Prostate cancer | 20668451 | CNVD |
Autism | 22495311 | CNVD |
Cancer | 20164919 | CNVD |
Bipolar disorder | 19114987 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
Lung cancer | 18438408 | CNVD |
Breast cancer | 22522925 | CNVD |
Rectal cancer | 20877625 | CNVD |
cervicovaginal lavage | 20877625 | CNVD |
Melanoma | 20877625 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:560600-561200 | Enhancers | Fetal Lung | lung |
2 | chr3:561200-562200 | Weak transcription | Fetal Lung | lung |
3 | chr3:562600-562800 | Enhancers | Fetal Lung | lung |
4 | chr3:563400-564600 | Weak transcription | Aorta | Aorta |
5 | chr3:564200-564800 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
6 | chr3:564600-564800 | Enhancers | Aorta | Aorta |
7 | chr3:577000-578800 | Active TSS | ES-I3 Cell Line | embryonic stem cell |
8 | chr3:577200-577600 | Enhancers | Esophagus | oesophagus |
9 | chr3:577200-579000 | Active TSS | Brain Hippocampus Middle | brain |
10 | chr3:577400-577600 | ZNF genes & repeats | HUES6 Cell Line | embryonic stem cell |
11 | chr3:577400-577600 | ZNF genes & repeats | Fetal Intestine Small | intestine |
12 | chr3:577400-577800 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
13 | chr3:577400-578000 | Active TSS | iPS-15b Cell Line | embryonic stem cell |
14 | chr3:577400-578200 | ZNF genes & repeats | Lung | lung |
15 | chr3:577400-578400 | Active TSS | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
16 | chr3:577400-578400 | Active TSS | HSMMtube | muscle |
17 | chr3:577400-578600 | Active TSS | HUES48 Cell Line | embryonic stem cell |
18 | chr3:577400-578600 | Active TSS | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
19 | chr3:577400-578600 | Active TSS | Fetal Intestine Large | intestine |
20 | chr3:577400-578800 | Active TSS | Foreskin Keratinocyte Primary Cells skin02 | Skin |
21 | chr3:577400-578800 | Active TSS | Colon Smooth Muscle | Colon |
22 | chr3:577400-578800 | Active TSS | Fetal Muscle Trunk | muscle |
23 | chr3:577400-578800 | Active TSS | Rectal Smooth Muscle | rectum |
24 | chr3:577400-578800 | Active TSS | Skeletal Muscle Female | skeletal muscle |
25 | chr3:577400-579000 | Active TSS | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
26 | chr3:577400-579000 | Active TSS | Foreskin Keratinocyte Primary Cells skin03 | Skin |
27 | chr3:577400-579000 | Active TSS | Fetal Kidney | kidney |
28 | chr3:577400-579000 | Active TSS | Pancreatic Islets | Pancreatic Islet |
29 | chr3:577400-579000 | Active TSS | Stomach Smooth Muscle | stomach |
30 | chr3:577400-579000 | Active TSS | NHLF | lung |
31 | chr3:577600-578200 | Active TSS | Primary hematopoietic stem cells short term culture | blood |
32 | chr3:577600-578200 | Active TSS | Esophagus | oesophagus |
33 | chr3:577600-578200 | Bivalent/Poised TSS | Fetal Adrenal Gland | Adrenal Gland |
34 | chr3:577600-578200 | Active TSS | Fetal Brain Female | brain |
35 | chr3:577600-578400 | Active TSS | HUES6 Cell Line | embryonic stem cell |
36 | chr3:577600-578400 | Active TSS | IMR90 fetal lung fibroblasts Cell Line | lung |
37 | chr3:577600-578400 | Active TSS | Cortex derived primary cultured neurospheres | brain |
38 | chr3:577600-578400 | Bivalent/Poised TSS | Foreskin Melanocyte Primary Cells skin01 | Skin |
39 | chr3:577600-578400 | Active TSS | Adipose Nuclei | Adipose |
40 | chr3:577600-578400 | Active TSS | Psoas Muscle | Psoas |
41 | chr3:577600-578400 | Active TSS | HSMM | muscle |
42 | chr3:577600-578600 | Active TSS | ES-WA7 Cell Line | embryonic stem cell |
43 | chr3:577600-578600 | Active TSS | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
44 | chr3:577600-578600 | Active TSS | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
45 | chr3:577600-578600 | Active TSS | Muscle Satellite Cultured Cells | -- |
46 | chr3:577600-578800 | Active TSS | Aorta | Aorta |
47 | chr3:577600-578800 | Active TSS | Duodenum Smooth Muscle | Duodenum |
48 | chr3:577600-578800 | Active TSS | Fetal Intestine Small | intestine |
49 | chr3:577600-578800 | Active TSS | Fetal Lung | lung |
50 | chr3:577600-578800 | Active TSS | Fetal Muscle Leg | muscle |