| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00258 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:8959460-8960610 |
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 | GTCTTATTTT TTTTATTTTT TTATTTTTTG AGACAAAGTC TTGCTCTTCT CCCCCAGGCT 60
GGAATGCAGT GTTGCCATCT TGGCTCACTG CAACCTCTGT CTCCCGGATT CAAGCAATTC 120
TCCTGCTTCG CCCCCTCAAG TAGCTGGGAT TACAGGTGCC CACCACCACG CGTGGCTAAT 180
TTTTGTATTT TTAGTAGAAG CGGGGTTTCA CCATGTTGGC CAGGCTGGTC TAGAACTCCT 240
GACCTCAGGT GATCTACCCG TTTCGGCCTC CTGAAGTACT GGGATTAGAG GCATGAGCCA 300
CCGTGCCCGG CCGTCTTTTG CTTTATTTTT GAGACAGAGT CTCACTCTGC TGCCCAGGCT 360
GGAGTGCAGT GGTGCTATCT CGGCTCACTG CAACCTCTGC CTCCCCGGTT CCAGTGATTT 420
TTGTGCCTCA GCCTCCCGAG TAGCTGCTGT GATTACTACA GGTGCCCACC ACCACGCCTG 480
GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGCTCAGG TTTGTCTCAA 540
ACTCCTGGCC CCAGGTGATC TGCCTGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGCAT 600
GAGCCACTGA GCCTGGCCTC TATATAAGCC CTAAGTTCTA ACCGCTCCTC TGAGTTACTC 660
ATCACTGAAT TTCCGTTGCA GGTGATTCAT GAGTTTCCAG GAAAGGGGTG GGTGATTTCC 720
AGAATGAGGG TTCCTCCCCT TTTTAGACTA TATAGGTAAA CTTCTGGGCC AGGCATGGTG 780
GCTCATGCCT GTAATCTCAG CACTTTGGAA GGCCAAGGCT GGCAGATCAC TTGAGGTCAG 840
GAGTTCAAGG ACAGCCTGGC AAGCATGGAG AAATCCTGTC TCTACTAAAA ATACAAAAAT 900
TAGCTGGGCG TGATGATGTG CTCCTGTACT CCCAGTTACT CAGGCAGCTG AGGCAGGAGA 960
AGCCGGAGGC AGAGGTTGTG GTGAGCCAAG ATTGTGCCAC TGCACTCCAG CCTGGGTGAC 1020
AGAGCAAGAC CCTGTCTCAA TAAACTAAAC TAAACTAAAA TAAATAAATA AAGGAATAGA 1080
CTACATAGGC TAACTTCTGG ATGTGGCTGT GGCATTTGTA AACTGTCATG GCGCTGATGA 1140
GAGTGTCTTT 1150
|
