| Tag | Content |
|---|
EnhancerAtlas ID | HS113-00197 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:8959020-8960770 |
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 | AGGAAGAAAC TCCGGACACA TCTGAACATC TGAAGGAATA AACTCTGGAC AAACCATCTT 60
TAAGAGCTGT AACAATCACC GCAAGGGTCC ACAGCTTCAT TCTTGAAGTC AGCGAGACCA 120
GGAACCCACC GGAAAGAATA AATTCCGGAC ACAACATTTC TTTTTTCTTT GAGACAGGGT 180
CTCAGTGGCA CAATCATAGC TCACTGCAGC CTCAACCTCC TGGGCTCAAG AGATCCTCCT 240
GCCTCAGTCT CCTGAGTAGC TGGCACACCG CCATGCCCTG CCAATTTTTT TTGTAGAGAC 300
AGGGGTCTCA CTGTGCTGCC TACACTGGTC TCGAGCTCCT GGTCTCAAGC AGTCCTCCCT 360
CCTGGTCGTC CCAAAGTGCT GGGATTATAG GTGTGAGCCA CCGTGCCTGG CCTCTTTTCT 420
TCTTTTTTCC CTCCACATGT GTCTTATTTT TTTTATTTTT TTATTTTTTG AGACAAAGTC 480
TTGCTCTTCT CCCCCAGGCT GGAATGCAGT GTTGCCATCT TGGCTCACTG CAACCTCTGT 540
CTCCCGGATT CAAGCAATTC TCCTGCTTCG CCCCCTCAAG TAGCTGGGAT TACAGGTGCC 600
CACCACCACG CGTGGCTAAT TTTTGTATTT TTAGTAGAAG CGGGGTTTCA CCATGTTGGC 660
CAGGCTGGTC TAGAACTCCT GACCTCAGGT GATCTACCCG TTTCGGCCTC CTGAAGTACT 720
GGGATTAGAG GCATGAGCCA CCGTGCCCGG CCGTCTTTTG CTTTATTTTT GAGACAGAGT 780
CTCACTCTGC TGCCCAGGCT GGAGTGCAGT GGTGCTATCT CGGCTCACTG CAACCTCTGC 840
CTCCCCGGTT CCAGTGATTT TTGTGCCTCA GCCTCCCGAG TAGCTGCTGT GATTACTACA 900
GGTGCCCACC ACCACGCCTG GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTCACCAT 960
GTTGCTCAGG TTTGTCTCAA ACTCCTGGCC CCAGGTGATC TGCCTGCCTT GGCCTCCCAA 1020
AGTGCTGGGA TTACAGGCAT GAGCCACTGA GCCTGGCCTC TATATAAGCC CTAAGTTCTA 1080
ACCGCTCCTC TGAGTTACTC ATCACTGAAT TTCCGTTGCA GGTGATTCAT GAGTTTCCAG 1140
GAAAGGGGTG GGTGATTTCC AGAATGAGGG TTCCTCCCCT TTTTAGACTA TATAGGTAAA 1200
CTTCTGGGCC AGGCATGGTG GCTCATGCCT GTAATCTCAG CACTTTGGAA GGCCAAGGCT 1260
GGCAGATCAC TTGAGGTCAG GAGTTCAAGG ACAGCCTGGC AAGCATGGAG AAATCCTGTC 1320
TCTACTAAAA ATACAAAAAT TAGCTGGGCG TGATGATGTG CTCCTGTACT CCCAGTTACT 1380
CAGGCAGCTG AGGCAGGAGA AGCCGGAGGC AGAGGTTGTG GTGAGCCAAG ATTGTGCCAC 1440
TGCACTCCAG CCTGGGTGAC AGAGCAAGAC CCTGTCTCAA TAAACTAAAC TAAACTAAAA 1500
TAAATAAATA AAGGAATAGA CTACATAGGC TAACTTCTGG ATGTGGCTGT GGCATTTGTA 1560
AACTGTCATG GCGCTGATGA GAGTGTCTTT TAGCATGCTA ATGTATTATA ATTAATGTAT 1620
ACTGAGTAGG GAGGACTACC AGAGGTCACT TTCATTGCCA TCTTGGTTTT GGCTGGTTTG 1680
GGCTGAGTTC TTTTTTTTTT TTTGAGACAG AGTCTCACTC TGTCACCCAG GCTGGAGTGC 1740
AGTGGCACAG 1750
|
