| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00282 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:8959170-8960690 |
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 | ACAACATTTC TTTTTTCTTT GAGACAGGGT CTCAGTGGCA CAATCATAGC TCACTGCAGC 60
CTCAACCTCC TGGGCTCAAG AGATCCTCCT GCCTCAGTCT CCTGAGTAGC TGGCACACCG 120
CCATGCCCTG CCAATTTTTT TTGTAGAGAC AGGGGTCTCA CTGTGCTGCC TACACTGGTC 180
TCGAGCTCCT GGTCTCAAGC AGTCCTCCCT CCTGGTCGTC CCAAAGTGCT GGGATTATAG 240
GTGTGAGCCA CCGTGCCTGG CCTCTTTTCT TCTTTTTTCC CTCCACATGT GTCTTATTTT 300
TTTTATTTTT TTATTTTTTG AGACAAAGTC TTGCTCTTCT CCCCCAGGCT GGAATGCAGT 360
GTTGCCATCT TGGCTCACTG CAACCTCTGT CTCCCGGATT CAAGCAATTC TCCTGCTTCG 420
CCCCCTCAAG TAGCTGGGAT TACAGGTGCC CACCACCACG CGTGGCTAAT TTTTGTATTT 480
TTAGTAGAAG CGGGGTTTCA CCATGTTGGC CAGGCTGGTC TAGAACTCCT GACCTCAGGT 540
GATCTACCCG TTTCGGCCTC CTGAAGTACT GGGATTAGAG GCATGAGCCA CCGTGCCCGG 600
CCGTCTTTTG CTTTATTTTT GAGACAGAGT CTCACTCTGC TGCCCAGGCT GGAGTGCAGT 660
GGTGCTATCT CGGCTCACTG CAACCTCTGC CTCCCCGGTT CCAGTGATTT TTGTGCCTCA 720
GCCTCCCGAG TAGCTGCTGT GATTACTACA GGTGCCCACC ACCACGCCTG GCTAATTTTT 780
GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGCTCAGG TTTGTCTCAA ACTCCTGGCC 840
CCAGGTGATC TGCCTGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACTGA 900
GCCTGGCCTC TATATAAGCC CTAAGTTCTA ACCGCTCCTC TGAGTTACTC ATCACTGAAT 960
TTCCGTTGCA GGTGATTCAT GAGTTTCCAG GAAAGGGGTG GGTGATTTCC AGAATGAGGG 1020
TTCCTCCCCT TTTTAGACTA TATAGGTAAA CTTCTGGGCC AGGCATGGTG GCTCATGCCT 1080
GTAATCTCAG CACTTTGGAA GGCCAAGGCT GGCAGATCAC TTGAGGTCAG GAGTTCAAGG 1140
ACAGCCTGGC AAGCATGGAG AAATCCTGTC TCTACTAAAA ATACAAAAAT TAGCTGGGCG 1200
TGATGATGTG CTCCTGTACT CCCAGTTACT CAGGCAGCTG AGGCAGGAGA AGCCGGAGGC 1260
AGAGGTTGTG GTGAGCCAAG ATTGTGCCAC TGCACTCCAG CCTGGGTGAC AGAGCAAGAC 1320
CCTGTCTCAA TAAACTAAAC TAAACTAAAA TAAATAAATA AAGGAATAGA CTACATAGGC 1380
TAACTTCTGG ATGTGGCTGT GGCATTTGTA AACTGTCATG GCGCTGATGA GAGTGTCTTT 1440
TAGCATGCTA ATGTATTATA ATTAATGTAT ACTGAGTAGG GAGGACTACC AGAGGTCACT 1500
TTCATTGCCA TCTTGGTTTT 1520
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