Tag | Content |
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EnhancerAtlas ID | HS052-34267 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr7:1231510-1232640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr7:1232069-1232082 | ACGATGATGTCAT | + | 6.64 | JUND(var.2) | MA0492.1 | chr7:1232068-1232083 | TACGATGATGTCATT | + | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 1231614 | 1232542 | chr7 | 1231899 | 1232263 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I001191 | chr7 | 1231625 | 1232609 |
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Enhancer Sequence | CTCCTTATGA GAATCTAATG CCTGATGATC TGTCATTGTC TCCCATCACC CACAGATGGG 60 ACCGTCTAGT TGCAGGAAAA GAAGCTCAGG GCTCCCACTG ATTCTACACG ATGGCGAGTC 120 GTAGAATTAT TTCATTCTAT ATCACAGTGT AATAACAGTA GAAGTAAAGT GCAACATAAA 180 TCGAATGTGC TTGAATCCTC CCGAAACCAT CCCCTGCCCC CACTGTCCGT GGAAAAATTG 240 TCTTCCACAA AACTGGTCCC TAGTCTCAGA AAGGTTGGGG CTCCCTGCTA TTGATGACCC 300 CCAGGCATCT CCCCAGCCTG CCTGCAGCTC CCTGTCCCTC TCACCGCAGC CGCCCTGGTC 360 CAGGCCGCGT CCTCTCTCCC CAGCCAACCT GCCTGCTGCT GTACCCCATC CGTCTCACTG 420 CAGCCATCCT GGTCCAGGCC GCGTCCTCCT CCCTAGGACA GCTGTGATGC TTCCCAGCTG 480 GACTTCCTGC TTCTGCCTTT ACCCTATAAC ATCCTTCTTT AACACAACGG CCAGAATGAT 540 TTCCTTCAAA AACAGCAATA CGATGATGTC ATTTGGCCGT TTAAAACTTC CTGTGGCTTC 600 ACGTTAGTCA GAGTCTAAAC AGGAAAACAG AGCCGCCTTC AGGTTGTGTA ACCAAAAGGG 660 AGTTGAAGGT GGGGAGTCGT TTACTAGCTT GGGGCAATCT ACACGCAACC TGGGGACATG 720 GGGAGCACCA GCAGGGACCC TCAGTCACCT GCAGAGTGGG GAGGCACCAG AACAAATGGA 780 ACCGAGGCCA CAGGTGTGCA GGCCCGCACC CGAAACCCCA ACACTGTGGG AGGCCAAGGT 840 GAGAGGATCG TTTGAGGCCA GGAGTTCGAG ACCAGCCTGG CCAACAGAGA GAGACCCCAT 900 GTCTATAAAA TATTTAAAAA TTAGCTGGGC GTGTTGGCTC ATGCCTGTAG TCCCAGCTAC 960 CCAGGAGGCT GAGGTGGAAG GATTACCTGA ACTCCAGAGG TTGAGGCTGC AGTGAGCTAT 1020 TAATACAATT GCACAACTGC CCTCCAGCCT GGGCAACACA GAGCAAGACC CTGTCACCCA 1080 CCCCCCACCA ACAAAAAATC AAAAAGCAAA AAACAAAAAT GAGCTGAGTG 1130
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