| Tag | Content |
|---|
EnhancerAtlas ID | HS061-00159 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:8959500-8960620 |
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 | TTGCTCTTCT CCCCCAGGCT GGAATGCAGT GTTGCCATCT TGGCTCACTG CAACCTCTGT 60
CTCCCGGATT CAAGCAATTC TCCTGCTTCG CCCCCTCAAG TAGCTGGGAT TACAGGTGCC 120
CACCACCACG CGTGGCTAAT TTTTGTATTT TTAGTAGAAG CGGGGTTTCA CCATGTTGGC 180
CAGGCTGGTC TAGAACTCCT GACCTCAGGT GATCTACCCG TTTCGGCCTC CTGAAGTACT 240
GGGATTAGAG GCATGAGCCA CCGTGCCCGG CCGTCTTTTG CTTTATTTTT GAGACAGAGT 300
CTCACTCTGC TGCCCAGGCT GGAGTGCAGT GGTGCTATCT CGGCTCACTG CAACCTCTGC 360
CTCCCCGGTT CCAGTGATTT TTGTGCCTCA GCCTCCCGAG TAGCTGCTGT GATTACTACA 420
GGTGCCCACC ACCACGCCTG GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTCACCAT 480
GTTGCTCAGG TTTGTCTCAA ACTCCTGGCC CCAGGTGATC TGCCTGCCTT GGCCTCCCAA 540
AGTGCTGGGA TTACAGGCAT GAGCCACTGA GCCTGGCCTC TATATAAGCC CTAAGTTCTA 600
ACCGCTCCTC TGAGTTACTC ATCACTGAAT TTCCGTTGCA GGTGATTCAT GAGTTTCCAG 660
GAAAGGGGTG GGTGATTTCC AGAATGAGGG TTCCTCCCCT TTTTAGACTA TATAGGTAAA 720
CTTCTGGGCC AGGCATGGTG GCTCATGCCT GTAATCTCAG CACTTTGGAA GGCCAAGGCT 780
GGCAGATCAC TTGAGGTCAG GAGTTCAAGG ACAGCCTGGC AAGCATGGAG AAATCCTGTC 840
TCTACTAAAA ATACAAAAAT TAGCTGGGCG TGATGATGTG CTCCTGTACT CCCAGTTACT 900
CAGGCAGCTG AGGCAGGAGA AGCCGGAGGC AGAGGTTGTG GTGAGCCAAG ATTGTGCCAC 960
TGCACTCCAG CCTGGGTGAC AGAGCAAGAC CCTGTCTCAA TAAACTAAAC TAAACTAAAA 1020
TAAATAAATA AAGGAATAGA CTACATAGGC TAACTTCTGG ATGTGGCTGT GGCATTTGTA 1080
AACTGTCATG GCGCTGATGA GAGTGTCTTT TAGCATGCTA 1120
|
