Tag | Content |
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EnhancerAtlas ID | HS105-12660 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr11:6378210-6379600 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr11:6378617-6378628 | GATGAGTCACA | - | 6.14 | JUND | MA0491.1 | chr11:6378617-6378628 | GATGAGTCACA | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I006356 | chr11 | 6377609 | 6379610 |
| Enhancer Sequence | AGATACACAA TAAGCCCCAA TAACTGCTAT TAAAAATACA TGCATGAGGC TTAACAGTGA 60 CACACTAAGT TACCCCTATA ATAATGTCCC CATCACTAAC TGGGGAGAAG AGGGAGTGGC 120 ATCACAGCCA GCTCTCAGGA ATTGCTTCTC CAAAACCTTT GCTACACGTG CACCCAGCAG 180 TGGTAGGAAG ATTGCTAACA CACCAATTGT CATGTCATTT TCAAGTCATC GTATTGCATT 240 GAAATGTAAT AGTTATTTTT GCCATTGGCT TTGATTTCCT TCCAAAATTC TTCCAGGGTT 300 TCGATAAAAT TGGGTTTAAC CTTTGAGAGT GCGTATGAAT ATGGTTGTCA TCCATTGTGT 360 GTGGGTGGTG GAGAAAAGAT TGAGAATGGC CGCCGTGCAC GGCTGAGGAT GAGTCACAAT 420 CTTTAGACCA GAAAGGGAGC TGAGTGGGAG GCCTGGCAGG AGAGAGTCGC AAGTATGAAT 480 CGGGGCTTTT GGCCCTGAGG CAATAATGAT GTCACGCCAT CTCTCCAATG TGGCCTCCCA 540 GTGAGATGTC CTGATCTAGC CAGGCCTGGA ACCTAGTGGA GAGGCGCCAG AAAGCCCAGT 600 GCCAGGGTCT CCTTATTGTG TGATCCAAAA CCTGTGCTTT GGAAATTTGA CGTAGGTGAG 660 CTATTTATAT TTTATATGTT CTCTTCCTCT CTGTTCTGCA GAAAAAACTT CATAAAATGC 720 CATCTATATC TGTACTTTCT TCATTGAATA TGTATTGCTT GTTTAATTTT TTAAAGATAT 780 GGATTCAAAG TAATACAGTA TAAAGAAAAG ACCCTAAAAT GAAAATGCCA GTTCAAACTG 840 TGTTCAGACG AATTAAAGTT TTGTTCACAT TCCTGGGAAA GCTGTAAAAA AGGAACAGCC 900 CAACTCCAAT TAGGAGTTGG GGACAAGGCT GGGCAAGCAG TTAGTTTTGA AGTCAGAAAA 960 CTCTCAGACT GCTGAGGAAA GAGGTGGGGA TAGGCGTGGG AATTTCAGAG CCCTTGCCCT 1020 GCTCCCCCTG CCGCAGAATT CTCCTTCCAG AACTCCCCTG TGCCAGACTT TCCTAAGTTC 1080 CACAGTGGTA TGCTTCCATG AGTAAAGTTG TTTCCATTAC TGACAGATTA TGGTGACCCA 1140 AGAGACATTT AGAATCCAGT TCTAGGCCTC AGAAGCTCTG TAAAGTCAGG GGACACAGGA 1200 GAGGCCAGTA GGCAGGGAAT GCCACACAAA TGTGAGCATC TCTTCCTTCC ATCTCTTTAA 1260 AGTCTATCTT CAAGAACAAG CCCACACTCT ACCTCCCTTG TGAAATTCTC CCTGACTCTT 1320 TGGCCACCAC TGGCCTCTCC TTCCTGGAGT TCTTTAATTA TGAAGATTAA GCACCATTTT 1380 ATGTCTTTCT 1390
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