Tag | Content |
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EnhancerAtlas ID | HS136-17755 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr7:1231410-1232810 |
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 | ACCGCCTGAG CTCCACCTTG TCAGATCAGT AGCGGAGTTC GATTCTCACA GGATCGTGAA 60 CCCCATTGTG AACTGTGCAT GCGAGGGGTT AGGTTTCACA CTCCTTATGA GAATCTAATG 120 CCTGATGATC TGTCATTGTC TCCCATCACC CACAGATGGG ACCGTCTAGT TGCAGGAAAA 180 GAAGCTCAGG GCTCCCACTG ATTCTACACG ATGGCGAGTC GTAGAATTAT TTCATTCTAT 240 ATCACAGTGT AATAACAGTA GAAGTAAAGT GCAACATAAA TCGAATGTGC TTGAATCCTC 300 CCGAAACCAT CCCCTGCCCC CACTGTCCGT GGAAAAATTG TCTTCCACAA AACTGGTCCC 360 TAGTCTCAGA AAGGTTGGGG CTCCCTGCTA TTGATGACCC CCAGGCATCT CCCCAGCCTG 420 CCTGCAGCTC CCTGTCCCTC TCACCGCAGC CGCCCTGGTC CAGGCCGCGT CCTCTCTCCC 480 CAGCCAACCT GCCTGCTGCT GTACCCCATC CGTCTCACTG CAGCCATCCT GGTCCAGGCC 540 GCGTCCTCCT CCCTAGGACA GCTGTGATGC TTCCCAGCTG GACTTCCTGC TTCTGCCTTT 600 ACCCTATAAC ATCCTTCTTT AACACAACGG CCAGAATGAT TTCCTTCAAA AACAGCAATA 660 CGATGATGTC ATTTGGCCGT TTAAAACTTC CTGTGGCTTC ACGTTAGTCA GAGTCTAAAC 720 AGGAAAACAG AGCCGCCTTC AGGTTGTGTA ACCAAAAGGG AGTTGAAGGT GGGGAGTCGT 780 TTACTAGCTT GGGGCAATCT ACACGCAACC TGGGGACATG GGGAGCACCA GCAGGGACCC 840 TCAGTCACCT GCAGAGTGGG GAGGCACCAG AACAAATGGA ACCGAGGCCA CAGGTGTGCA 900 GGCCCGCACC CGAAACCCCA ACACTGTGGG AGGCCAAGGT GAGAGGATCG TTTGAGGCCA 960 GGAGTTCGAG ACCAGCCTGG CCAACAGAGA GAGACCCCAT GTCTATAAAA TATTTAAAAA 1020 TTAGCTGGGC GTGTTGGCTC ATGCCTGTAG TCCCAGCTAC CCAGGAGGCT GAGGTGGAAG 1080 GATTACCTGA ACTCCAGAGG TTGAGGCTGC AGTGAGCTAT TAATACAATT GCACAACTGC 1140 CCTCCAGCCT GGGCAACACA GAGCAAGACC CTGTCACCCA CCCCCCACCA ACAAAAAATC 1200 AAAAAGCAAA AAACAAAAAT GAGCTGAGTG TGGTGGCTTA AGCCTGTAAT TCCAGCACTT 1260 TGGGAGGCCA AGGCATGAGG ATCACTTGAG CTCAGGAGCT TGAGACCAGC CTGGCCAACA 1320 TGGTGAAACC CCATCTCAAC TAAAAAAAAT ACAAAATTAG CTGGGCATGA TGGTGGGCGC 1380 CTGTAATCCC AGCTACATGG 1400
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