Tag | Content |
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EnhancerAtlas ID | HS176-15767 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:963760-964900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr17:964771-964787 | GTTTGTTTACTAAGTG | - | 6.2 | Foxd3 | MA0041.1 | chr17:964767-964779 | AATTGTTTGTTT | + | 6.22 | KLF13 | MA0657.1 | chr17:964338-964356 | CAGCAAGGGGCGTGTCTG | - | 6.28 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23794 | chr17:964347-964722 | Colon_Crypt_2 | SE_26634 | chr17:964281-964943 | Esophagus | SE_40640 | chr17:963477-964104 | Left_Ventricle | SE_40640 | chr17:964150-964976 | Left_Ventricle | SE_65254 | chr17:963488-965210 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I001060 | chr17 | 963683 | 965009 |
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Enhancer Sequence | GCGCACACCA GCATAAGCAA AGAAGAGTTC AGAAGAATAC ACCTCAAACT GTCAGCAGTG 60 GGAGGTGAGT GGCGACCAGC TTTACCCTGT ACATGCTGGT ACTACGAGCA TTTCTCATTA 120 AAACCAGCCA GTATTATATT GGGGATTAGA AAAAACATGA AAATTTAAAA AATTATTATC 180 AAGAGAACAA GGCTGAGCAC GGTGGCTCAC ACCTGTCATC CCAGCACTTT GGGAGGCCGG 240 GGCGGGTGGA TCATGAGGTC AGGAGTTTGA GACCAGCCTG GCTAACACGG TGAAACCCCG 300 TCTCTACTAA AAATACAAAA AATTAGCCAG GCGTGGTGGC GGACGCCTTT ATTCCCAGCT 360 ACTCAGGAGG CTGAGGTAGA AGAATTGCTT GAACCCGGGA GGTGGAGGTT GCAGTGAGCC 420 GAGATTGTGC CACTGCACTC CAGCCTGGGC GACAGTGACA AAGTGAGACT CCATCTCAAA 480 AAAAAACAAA AAACAAAAAA CAAATCACTG CTTCTTCTGT GACTCAGAGG ACGGCACCTG 540 TGCCTCTCCA GTGACTCACA TGTACCACAC TCTGTGGTCA GCAAGGGGCG TGTCTGCTTC 600 CTCCACTGGA CAGGGATATA CATGAGGCAC CCGGCACACC CCAGGCAGCA CAGCCAGTGG 660 GGCTCACTGA GTGTTGACTG TTGACTCGAC TGGGCACAAG GCCACGTCTG CACAGCTGGG 720 GCAACGGGGA GGCAGCAAGC CTCCCAGGGG CGGGTGGGAA ACAGGCACGC AGGATGCTCC 780 TGGGCGGGCA CTGTGGGCAG GGCCCAGCCG TTCAGGAGGG GGACAGCTGT GCTGGCGAGG 840 AAGCCCTCTG GGCAGATGTA CCACCAGTTG GACCCTCTGT CCTAGGACAT CCCCCAGCCC 900 TGAACACTCC TGGGGCTGTA ATGGTGATCT TGCTTTCCCC TGTTCAAAGG GAGATGCTTG 960 AGTTGAAAGG ATCCTCAGAG AGGCCATCTG GTTATGTTTT CTTCAATAAT TGTTTGTTTA 1020 CTAAGTGCCT TTTTTTTTTT GAGATGGAGT CCCACTCACT CTGTTGCCCA GGCTGGAGTG 1080 CAGTGGCGTG ATCTCGGCTC ACTGCAACCT CCACCTCCCG GGTTCACACA ATTCTTTTGC 1140
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