| Tag | Content |
|---|
EnhancerAtlas ID | HS073-00082 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:8959440-8960820 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:8960292-8960307 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr5a2 | MA0505.1 | chr1:8960300-8960315 | GAGTTCAAGGACAGC | + | 7.06 | | RARA | MA0729.1 | chr1:8960292-8960310 | GAGGTCAGGAGTTCAAGG | + | 6.73 | | STAT1 | MA0137.3 | chr1:8960153-8960164 | TTTCCAGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr1:8960153-8960167 | TTTCCAGGAAAGGG | + | 7.64 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_27088 | chr1:8959478-8960765 | Esophagus | | SE_34103 | chr1:8959575-8960842 | HCC1954 | | SE_34433 | chr1:8958839-8961107 | HCT-116 | | SE_34916 | chr1:8959109-8961267 | HeLa | | SE_36553 | chr1:8959977-8960884 | HMEC | | SE_46612 | chr1:8959902-8960819 | Osteoblasts | | SE_47312 | chr1:8959436-8960657 | Panc1 | | SE_56056 | chr1:8958921-8961024 | u87 | | SE_67633 | chr1:8958921-8961024 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I008899 | chr1 | 8959185 | 8960724 |
|
Enhancer Sequence | TCTTTTTTCC CTCCACATGT GTCTTATTTT TTTTATTTTT TTATTTTTTG AGACAAAGTC 60
TTGCTCTTCT CCCCCAGGCT GGAATGCAGT GTTGCCATCT TGGCTCACTG CAACCTCTGT 120
CTCCCGGATT CAAGCAATTC TCCTGCTTCG CCCCCTCAAG TAGCTGGGAT TACAGGTGCC 180
CACCACCACG CGTGGCTAAT TTTTGTATTT TTAGTAGAAG CGGGGTTTCA CCATGTTGGC 240
CAGGCTGGTC TAGAACTCCT GACCTCAGGT GATCTACCCG TTTCGGCCTC CTGAAGTACT 300
GGGATTAGAG GCATGAGCCA CCGTGCCCGG CCGTCTTTTG CTTTATTTTT GAGACAGAGT 360
CTCACTCTGC TGCCCAGGCT GGAGTGCAGT GGTGCTATCT CGGCTCACTG CAACCTCTGC 420
CTCCCCGGTT CCAGTGATTT TTGTGCCTCA GCCTCCCGAG TAGCTGCTGT GATTACTACA 480
GGTGCCCACC ACCACGCCTG GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTCACCAT 540
GTTGCTCAGG TTTGTCTCAA ACTCCTGGCC CCAGGTGATC TGCCTGCCTT GGCCTCCCAA 600
AGTGCTGGGA TTACAGGCAT GAGCCACTGA GCCTGGCCTC TATATAAGCC CTAAGTTCTA 660
ACCGCTCCTC TGAGTTACTC ATCACTGAAT TTCCGTTGCA GGTGATTCAT GAGTTTCCAG 720
GAAAGGGGTG GGTGATTTCC AGAATGAGGG TTCCTCCCCT TTTTAGACTA TATAGGTAAA 780
CTTCTGGGCC AGGCATGGTG GCTCATGCCT GTAATCTCAG CACTTTGGAA GGCCAAGGCT 840
GGCAGATCAC TTGAGGTCAG GAGTTCAAGG ACAGCCTGGC AAGCATGGAG AAATCCTGTC 900
TCTACTAAAA ATACAAAAAT TAGCTGGGCG TGATGATGTG CTCCTGTACT CCCAGTTACT 960
CAGGCAGCTG AGGCAGGAGA AGCCGGAGGC AGAGGTTGTG GTGAGCCAAG ATTGTGCCAC 1020
TGCACTCCAG CCTGGGTGAC AGAGCAAGAC CCTGTCTCAA TAAACTAAAC TAAACTAAAA 1080
TAAATAAATA AAGGAATAGA CTACATAGGC TAACTTCTGG ATGTGGCTGT GGCATTTGTA 1140
AACTGTCATG GCGCTGATGA GAGTGTCTTT TAGCATGCTA ATGTATTATA ATTAATGTAT 1200
ACTGAGTAGG GAGGACTACC AGAGGTCACT TTCATTGCCA TCTTGGTTTT GGCTGGTTTG 1260
GGCTGAGTTC TTTTTTTTTT TTTGAGACAG AGTCTCACTC TGTCACCCAG GCTGGAGTGC 1320
AGTGGCACAG TCTCAGCTCA CTGCAATCTC CACCTCCCAG GTTCAAGTAA TTCTCCTGCC 1380
|
