Tag | Content |
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EnhancerAtlas ID | HS053-38008 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr8:8910110-8911500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr8:8910757-8910767 | CTCAAGTGGT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_56603 | chr8:8910695-8911982 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 8910791 | 8911200 | chr8 | 8911216 | 8911351 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I009052 | chr8 | 8910246 | 8911836 |
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Enhancer Sequence | GGGGCACAGT TGGCAAGGAG GTTAAATATG TTAACTTCAG GATACATTTA GGGAAACTGC 60 AATCAAGAGA TTTACCCAGA AAACACATTT CAGAACTATG GTATAATAAA AAATATGTTT 120 GGTCTTTATC CCTGACTCCT GGCACTGAGC ATCAAAGACC CTTGGAAATT TCCGAGTGGT 180 TCGAATGTCT GTTGTTATAC ATGAATCCTT TCTGATCATA ACTAAGTTTA TGCTATTGAG 240 GTGAATCAAG GTGGGCCCTT AAATAGTTTC AGGAGAGAGG CTGGCCACAC TACAAAGACC 300 AAGCTTATGA TTAGAGGGTT GGAACTTTTG GCTCCACCCC TCAACCTCTG GAGAGAAGAG 360 GGGAACTGGA GATTGAGTTC AATCACTAGT GGCTAATGAT TTATTTATTT TTGTTTTTGT 420 TTTTGTTTTT GTTTGAGACG GAGTCTTGCT CTGTCACCCA GGCTGGAGTG CAATGGCGCA 480 ATCTCAGCAG ACTGCAACCT CTGCCTCCCG GGTTCAAGAG ATTCTCCTGC CTCAGCCTCC 540 AGAATAGCTG GGACCACAGG CATGCACTAC CACACCTGGC TAATTTTCAT ATTTTTAGTA 600 GAGATGGGGT TTTGCCATGT TGGCCCCACT GGTCTCGAAC TCCTGACCTC AAGTGGTCCG 660 CCTGCCTTGG CCTCTCAAAT TGCTGGGATT ATAGGCAAGA GCCACCGCGC CCAGCCAGTG 720 GCTAATGATT TAGCTGATCA TGCCTAAGTC ATGACACCTC AATAAAAACT CTTGAGCAAC 780 AAGCTTCCAG GAGCTTCTGG GTTGATAAGC TCATGATGTG CTGGGAGGAT GGCATGCCCA 840 GAGAGGGAAT GGAAGCTCCA CAGCCCAGCC ACTAGCCCCA TACCTCGTCC TACACGTCTC 900 TTCCATTTGG CTGTTCTTGA GTCGTATCCT TTATGGGAAA CTGTATGTGA ATCATCAATA 960 CAGTGCTTTG TTGAGTTCTA TGAGTCACCG TAGTCTGTTA ATGAACCTGA AGCAGTCATG 1020 GAAACTCCTC AATTTATAGT CAGCCAGGTA GAAGTGCAGG TAGCCTGGGG ACCCCACTGG 1080 CCCTGGACGT TTTGTGGAAC TGAGGCCTTG GTTTGTGTGA TATGACAGTA ACTCCTGATA 1140 GTACCAGAAT TGAACTGTAG GACACCCAGT GAATGTTAGA GAATTGATGT TGAAACCCTA 1200 AGAACTTTGG AGGAACTGAT TGTAAGAATT CTCTTCTGAA AAGCAGCCAA GTCCTCTATT 1260 GCCTCCAGAG AACCACGTTC AAATCATTGA TAACAGAGTA TAGTATTCTC TTTCTCTGCT 1320 TTCTTCCTCT CTTTGGTGGT TTTCAACAGG TTGTTTGGAA GTGAAAGGAA ATATGTCTGT 1380 GATAGGGGGG 1390
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