| Tag | Content |
|---|
EnhancerAtlas ID | HS147-18769 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr17:77825960-77827260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr17:77826488-77826498 | CCCAATTAGC | + | 6.02 | | IRF1 | MA0050.2 | chr17:77826780-77826801 | TCGTTGTTTCACTTTCGTTTT | + | 7.53 | | IRF9 | MA0653.1 | chr17:77826784-77826799 | TGTTTCACTTTCGTT | - | 6.43 | | Nr2f6(var.2) | MA0728.1 | chr17:77827206-77827221 | TGAACTCCTGACCTC | - | 6.22 | | Zfx | MA0146.2 | chr17:77827231-77827245 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27416 | chr17:77826194-77826977 | Esophagus | | SE_28334 | chr17:77826276-77827375 | Fetal_Intestine | | SE_62183 | chr17:77773273-77827285 | Toledo |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I079852 | chr17 | 77826314 | 77827312 |
|
Enhancer Sequence | TGCAGATTAA ACTTAAAAGT GTGTCCTGTT GGCTGGGCAC GATGGCTCAC GCCTGCAATC 60
CCAGCACTTT GGGAGGCCAA GGCGGGCAGA TCACTTGAGG TCAGGAGTTC GAGACCAGCC 120
TGGTCAACAT GGTGAAACCC CGTCTCTACT ACAAATACAA AAATTAGCCG GGTGTGGTAG 180
CGTGGTAGCG GGCGCCTGTA ATCCCAGCTA CTCAGGAGGC TGAGGCAGGA GAATTGCTTG 240
AACCCAGGAG GCGGAGGTTG CAGTGAGCCC AGATTGCACC ACTGCACTCC AGCCTGGGTG 300
ACAATAGCGA GACTCCATCT CAAAAAACAA AACAAAACAA ACAAAAAAGT GTGTCCTGTT 360
TGTAGCCATT ATGTTCTTTT GTTCCTTCTT TTCTTCTTCT TCTTCTTTTT TTCTTTTTTT 420
TTTTTATACA GGGTCTCACT GTGTCACCCA GGCTGGAGGG CAGCGGCAAA ATTTTGGCTC 480
ACTGTGATCT GCAACTCTCG GGCTCAAGCA ATCCTCCCAC CTCAGCCTCC CAATTAGCTG 540
GGACTACAAG CGTGCACTTC CATGCCTGGC TAATATTTTT GTATTTTTTA GTACAGACGG 600
GTTTTTGCTG TGTTGTCCAG GCTGGTCTCA AACTCCTGGG CTCAAGTGAT CCAGTGGCCT 660
CGGTCTCTCA AAGTGGTGGG ACTACAGGCA TGAGCCACCA CACCCAGCCC ATTATGTTCC 720
TAAGAGCACA GGAATGGAGG AAGTAGTATT AAAAAACTAT TCCCTGATTT ATGAAAGAAG 780
TTCCTGACAT CATTATGAAC GAGAAGTTTG ACCTATTCCT TCGTTGTTTC ACTTTCGTTT 840
TACTGGTTAA CTTAAATGAA AATACCCACA GCCATTCAAG TCAGAACCAC ACTCATTTAT 900
CAAAGGCAAG CCTGGGCTGG CAACTGATCC CAGAGTTTGG CAAAAAAGCA ACAAAAACCT 960
TCTGTGAATC CATCAGTATA TGGAGCTTAC AATGAAGAGT ATCTTCTATT TTATTATTTG 1020
TTTATTTATT TTATTTTATT TTTTTGAGAT GGAGTTTCCC TCTTGCTGCC CAGGCTGGAG 1080
TGCAACGGTG TGATCTCAGC TCACTGCAAC CTCTGCCTGC CAGGTTCAAG TGATTCTCCC 1140
GTCTCAGCCT CCTGAGTAGC TGGGAATACC GGCATATGCC ACCATGCCTG GCTAATTTTG 1200
TATTGTTAGC AGAGACGGGG TTTCTCCGTG TTGGTCAGGC TGGTCTTGAA CTCCTGACCT 1260
CAGGTGATCT GCCCGCCTCG GCCTCCCAAA GTGATGGGAT 1300
|
