Tag | Content |
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EnhancerAtlas ID | HS062-02614 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr11:9036870-9038200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:9037325-9037344 | CAACCACTAGGTGGCACCT | + | 6.61 | Gfi1b | MA0483.1 | chr11:9037211-9037222 | AAATCACAGCC | + | 6.02 | ZNF263 | MA0528.1 | chr11:9037543-9037564 | CCTCCCACCACCTCCTCATTC | - | 6.11 |
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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 |
GH11I009015 | chr11 | 9037241 | 9037548 |
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Enhancer Sequence | GGGAGTGTGG TAGGGAGCTC CTGGAACTAC AAAGTGGTAA AACATGCAAG ATTATAATTG 60 AGGAGTAGAT TTTGTCCTCA TCATTCCTTC AACTCCTTTT CCCTTCTGAC TCAGGACTAT 120 ATATCCAGCC TACCCTGGTG CCTAGACCGT AACAGTGAAT GCATGAATAT GCGGTGTTTG 180 TATGTGAGAT TCAGAGCGTT GTTGATAGTT TGAAATGACC TAGATCAATG AGTTTGGACT 240 TGGTCACTAG TTTTTCTCTG CCAAGCAGAG AAAAAAGGAA AATATCTAAA CAAAATAAAC 300 TCCGAGGGCT GTGTCAAACA ACATGCGACC AATCAGTTGT CAAATCACAG CCCTAGTCCC 360 CAGGGCCCCT TGGGTAAGAT CTTGTCTTGA ATTATGGGCA TGTAAGGTCT GAGGCAGTGG 420 GACGGGAGAC AGAAACACAG GTCGACTCCA TATTGCAACC ACTAGGTGGC ACCTGTTCGA 480 GGAACTGCCA AATGGCTTGT TCACAGCTTG AAGCTTTGGT CAGCTTGGCT TGACATGAAA 540 TGCCAAGGTC TTGCTGGGCG GATAAAGGAG CTTGCCAGGG CCAGTGCTGC CAGGCTTGGT 600 TTGAGGAGCC AGTGCTCTAG GAGGGGCCTG GATTCATGAC TCTAATGATG AGCTCATCCT 660 AAGACAGCAG CTCCCTCCCA CCACCTCCTC ATTCTCTGTC CTTTAGCCCT TCCTTATTTA 720 TACCACTCAT CACTACTTGA CTTTACAGTA TATGTTCATT TGTTTATTGT CTGTCTCCCC 780 AGACTGGAAC CTAAATTCCA CAAGAGCAGG GAGCTTCTTT TGCTCCCTGC AGTATCCCTG 840 GCTCCTACAA TGTCTAGCAC TTAATAGGCT CTCCATAAAT ATATGTTGCA TAAATGAATG 900 AATGACCAAA AACATAATAA GAAATTATTA GTAACTAAGG TCTGTAGTTG CATCCCCTTT 960 ATGAGATACT CTGAAAACCA AGCACTACTG AGTTACTGTC ATTGCTTGCA GTAGGTAGGT 1020 TTAATTTGTA TCGCTTTTAT TCAACTAAGG CAAACTGCCT ATATTAGAGT GGTTTCATTT 1080 TCTAAATCTA TTTTGATGCC ACTGTGTTCT CTGGAAAGTG CTCCCTGCTG AGTAGTGATA 1140 TCTTCATGGC TATATCACTG ACATGGATCA CAGGAGCAGC CTTGCTGTGT TAACAGGTCC 1200 CTAAGGGTGG TCTCCTGCAG GCTGATCGAG ACTGCCTGAA GGGAGAAGGA GGCAGGGCAC 1260 TACAAATATT AGGACACCTC TGAGCTGGGC TCACAAGCCC CTGGAATGGA AGATGGTCAC 1320 AGAAATGAAG 1330
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