Tag | Content |
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EnhancerAtlas ID | HS053-41841 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chrX:38741910-38743180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chrX:38742121-38742134 | GATTAATTAATTT | - | 7.82 | POU6F1 | MA0628.1 | chrX:38742122-38742132 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chrX:38742122-38742132 | ATTAATTAAT | - | 6.02 | ZNF263 | MA0528.1 | chrX:38743022-38743043 | TCCTCCCACCCTCCTTCCTCT | - | 6.17 | ZNF263 | MA0528.1 | chrX:38743018-38743039 | CCCCTCCTCCCACCCTCCTTC | - | 7.09 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58717 | chrX:38704913-38797361 | Ly1 |
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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 |
GH0XI038882 | chrX | 38741819 | 38743290 |
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Enhancer Sequence | ACTCAGAAGT GGAATCAAGA TCTTTCTGAC CGCAAGATTT ATTTTCTTAT TTCAATTTAT 60 CATCTCTCAA GAAAGTGAGC TTTGGGATAA AAGAAAAATA AAACTGCCAG TTAAAGCTCT 120 ATGAACATGG TGAGGATATT TAAACATTTT GTCCTTTGGT TTTCTTCTCT GAAAAATGAA 180 AATAGCTCAG AAGAGTTGTG AAAATTAAAT GGATTAATTA ATTTAAAATC TCTGGCACAT 240 AGTAGGCACT CAATAAATGT TAGTTTCCTT CCTTTTTGAG AAAGCCACTT GGATTCCTTT 300 GCAGGATGGA AATCAAGGAA GCATTAGCTC AAGTTGAAGC TTTTCAGAGA TCTGAAACTA 360 ATACTGCCTG AGTTTTTCCA ACTCAGGAAG GAGGCTAGTG AAATATCACA GCCCTCAGCC 420 AGGTGGCCTG TTACTGAGTA AACCCTGATG GGAAATGGTG GCAGGGGACT ACTTCTGTTA 480 CACAGGGTAG CTGATATGCA AACATAAGTC ACTGTATTGC CATATAAAGA TTTAGTTCAT 540 AACCGTGTGA TACTATAGTT ACTTTGAGAG AAGAGAACTA AAAAAACTCA AGCTGTAGTC 600 CAGTGAAATT GTTCATTTTT GGTAAAAGAG ATTCTGGCAG TTTGAGACTC CATCCCTGGT 660 TGATTGTTGA AGCTTCCAGA GAATGAGTCC AGTGACTCCT CATCTCCTGT ACTATGATTG 720 GGCACTGAGT CACACTCCCA ACCCCACCCT GGCCCTCTAT GGCACTCCCC AACTGGCGTT 780 CCTGCAAGCT TTCCAAACCA GGGTACAGTC ATACTTCCCA CAAACCTGCT AAGGGCTTCC 840 TGGGACAGCG GATGCTTGAG GAGTGCTTGG TCAAGGCCTA GGTTTAAGTC GTGGTTTTGC 900 CTCAAGTGAG GGATAACTCT CAGCAGTCTT GCTCATAAGT CTTTTTGAAG AACCAACTTT 960 TTTTTTTTTT AACTTTTAAG TTCAGGGGTA CGTGTGCAGG TTTGTTATAT AGGTAAACTT 1020 GTGTTTACCT TGTGGGTTTT GTTGTACAGA TTATTTTGTC ACCCAGATAT TAAGCCTAGT 1080 GTACCAATAG TTATATTTCC TGATCCTCCC CCTCCTCCCA CCCTCCTTCC TCTGATAGGC 1140 CCCAGTGTCT GTTAGAACCA ACTTTTCACT TCTTGAGTAT CTCTATTGTC CGTTTATGTT 1200 CTTTGGCTTA TCTTTATTGT TTCCTTCCTT TTGCTTTCTC TGAATGTAAT GTGTTGTATT 1260 TTTCTTCTTG 1270
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