Tag | Content |
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EnhancerAtlas ID | HS147-13577 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr14:39687220-39688280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr14:39688187-39688199 | AAACAAACAAAC | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr14:39687972-39687987 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr14:39687693-39687708 | TGACCTCTTGAACTC | - | 7.14 | RARA | MA0729.1 | chr14:39687690-39687708 | ACTTGACCTCTTGAACTC | - | 7.14 |
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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 |
GH14I039216 | chr14 | 39685923 | 39689077 |
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Enhancer Sequence | CACCGAAAAC TGAAAATAAC TCAAAAGTCT GTCAACTAGA GAATGGATGA ACAAGCTGTT 60 GTACATCCAT ACAAATGGAC TACAGTTCAA CAATAAAAAG GAAAAAACAC ACACAAAGTA 120 AAATGTGACT ACTAGAAAAT TACATATGTG GCTCACTCTG TCTCTCTCTT TTTTTGTTGT 180 TTTTGTTTTT TCTTTAGAGA CGGGGTCTGG CTGTGTCACC CAGGATGGAG TGCAGTGGCA 240 CAATCGTAGC TCACTGCAGC CTCAATCTCC TAAGCTCAGG CAATCCTCCC ACCTCAGCCT 300 CTCAACACTC TCTATTTCTA TCGGACAATG CTGACTTAGA AGTTTTTGGC TTGATCTTTT 360 TGTGTTGGAG CAAAAGCAAA ATTACTTTTT GAGAAGATTC TTGGGCTGTC TCCAAGTGCT 420 CCTTTGGCTT ACTTTCAAGG TGGAGTTGGG AAGTGACTTT CTATTTAGTC ACTTGACCTC 480 TTGAACTCCT TACCTTTCAT AAGATAATAT CAGTCTTACC TCTACTCTGC TAAGAGTTAA 540 AAGTATATGA TTCAGCACTT AACAGGCCAT ATAGAAAGTT ACAGTCTACA TATTGTCAGC 600 GAACATGACC TCAGACTCAC AGTTGTTTGT TCAGTACTTA TCAATGTGAA AAAAATCACA 660 GTTTAATGTT CATTTAAAGA AGTCATGGCC AGGTACAGCG GCTCATGCCT GTAATCCCAG 720 TACTTTGGGA GGCCTAGGTG GGTGGATCAG TTGAGGTCAG GAGTTCAAGA CCAGCCTGGC 780 CAACATGGTG AAATACAAAA AATGCAAAAA TAAAAAATAA AAATAAATAA ATAAATAAAT 840 AAACAAATCC CAGCTACTTG GGAGGCTGAG GCAGAAGAAT CGCTTGAACC TGGGAGGCAG 900 AGGTTGCAGT GAGCTGAGAT CGTGCCACTG CACTCCAGCC TGGGCACACC ATGCAACTCC 960 GTCTCAAAAA CAAACAAACA AAAAAAACAA AAACAAAGTC ATGAAAACTG CTGAAATTAC 1020 AGAGGCAAGG ATAAGCATTT CATGGCTTTG GCAGGCCTAG 1060
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