| Tag | Content |
|---|
EnhancerAtlas ID | HS092-07887 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:119695050-119696830 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr10:119696015-119696033 | GAAAAGTGAAAGGAAACA | + | 6.49 | | ZNF263 | MA0528.1 | chr10:119695713-119695734 | CCTTCCCCGCCCTCGTCCTCC | - | 6.79 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I117935 | chr10 | 119695330 | 119696894 |
|
Enhancer Sequence | TTCACTCAGA ATGAAATGCA AACTCTTCCC TTCGACACTG AAGGTCCTCC TCAGTTTCAT 60
CCTTCTTTGT CTTTCCAGCG GGATCTCCTC CTTCCTCCCT CTGTCCCTTA CACACACAGG 120
CATGCACAGG TGCGTACGCA CACACACAGC ACATTCAAAA TTCCCTGAAA CACCACCTCC 180
AAGAATTCCC ATATTTTTCC TTTTTGAATG GAGGATCATG TGGTATAGGA AACAAAACAA 240
GCGTGGGCCC CCAAACGTTT TGCATTTGAA TTTTCGCCAT CTGTGGACTG TCTGACCTTG 300
GGTAATCCAT GTAGCCTCTA TCAGCCTGAC TTTACTTATC TACAGAATGA AGATAAAAAT 360
CATGCCCACT CTCAGAGTTG ATGAGATAGG ACATTTGTAA TGTGATTACT GTGTGGCTCC 420
TTGTGGCCCT CCAACTCAGT AGCTGATTTT CTAATCCTGG CCTGATTTGA TTGACTCCCT 480
ATCCCTTCTG CCCCAAGGTT TAGGAACACA GCTCGAGAAA ATGAAAGAGA GAGTCCTGAG 540
CAGACAGAGA TGAGCATGGC AGGAGCTCAG GGAGCAAATG GAGACTGGAA GCTGAAACAC 600
TGGGGTCAGC ACTAAGAGAG CAAGATGGGG GACTTCGTGC TGCAGCTTCC TGGCTTCCTG 660
GTTCCTTCCC CGCCCTCGTC CTCCTTCCTT CACTCACCGA TTCCAGGCCC TTTTAAGGCT 720
ACCCAGAGCA ACCTCGCCCA GTAAACTACA CTCTCTCAGG CCTTGACTGA GGCTGTGTTG 780
ACAACCACTA AAGTTGCCAC TTAACTCCAG CTCTTTAAAA GTCCGATTTC ATAACAGGAT 840
GATGTGATCC CGGCAGCATT TGCGAGGTGC AGCTGCCTGT GTGTAATCAG GCACAGACCA 900
CAGCAGTGTG CGTGGCAAGC ATTCTGTTCC AAAGTTTCCT TCAGTTTCTT GAATTCTATC 960
AGTCTGAAAA GTGAAAGGAA ACAGCACTGA AGGCCTTTAG GGTCAAGATA ATGGTGGGAA 1020
ATGACAGGGA ACTCCATCAA GAAATCAAAT ATCCACTGAA TTTATAATCC ATATTTAATA 1080
TGGATTAAAC ATTAGAGTAT TTCATCTCCA TGCTCACAGG CGTAATATTC TAATCGCACA 1140
GGGACTAAAT ACTGCCCCTT CCAAAAAGAA AATCTGCTCT GGTTCCTATG CAACTATGCA 1200
TCACTGTGTA TCCTAAACAC AGCCAACACA GTATAAAGGC TTAACACGTG GGCAGCTTTC 1260
CTCTGTGATC TGCCTTTGTG AACCTCCTTT CTGGTAATGG CTAACACACT TATGCTGAGA 1320
CATAGAGGGC CTCCTTTAGA AATGATCAAA GCTGTGAGAA AGAGAATTCA GGTGAGCACT 1380
GGCACATGAC TCTGGTGGGA TGACGTGCTT GAATCTGGCC CTGCAGCAAT AGAATTAGTT 1440
TTCGAAACAG AAGAGAACTA CAGATCTCTG TGTAGTTCAG TCTTCTTGCT CCTTTCTGAG 1500
GACATTTTCA TTCCACAGGG AATCTGGTCA CCATGCTGAA AGTTACCAGA GTGGGCTGAA 1560
ATCTCCCCAA CACACAAATG GCCAACATTC TTCATAGTAA TCCATTCTGC TCATAAGGAA 1620
GGAACCCAGG CTCCAGGGAC TCTGTTCCTC TCACAAGTGA TATTTTCCTA TAATAAACAC 1680
AGCAGCTGCC ATTTATTAAG CACATAGTAT GTGCCAAGCA CAATACTAAG AGCCTTACGT 1740
CATGGTCATT AGGTCGAATG GCAGGACAAT TATATTATAT 1780
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