Tag | Content |
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EnhancerAtlas ID | HS073-05812 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr17:4919660-4920720 |
Target genes | Number: 33 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:4919766-4919781 | TGAACTCCTGACCTT | - | 6.04 |
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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 |
GH17I005016 | chr17 | 4919691 | 4920772 |
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Enhancer Sequence | TTGACCTCCC AAGGTGCTGG GATTACAGGC TTGAGCCACC ACACCCAGCC CTAATTTTTG 60 TATTTTTAGT AGAGACAGGG TTTCACCATG TTGGTCAGGC TAGTCTTGAA CTCCTGACCT 120 TGTGATCCAC CTGCCTCGGC CTCCCAAAGT GCCAGGATTA CAGGCGTGAG CCACCGCACC 180 CGGCCAGCAC ATTTTAAAAA ATAACAAAAG ACGCTATCAT GTGCGTCTTA CAGTGAGGTT 240 TAAGACATAC CTCTTGGGGC TGGTGGGGTG GCTCATGCCT GTAATCTTAG CACTTTGGGA 300 GGCCGAGGTG GGTGGATCAC TTGAGGTCAG GAGTTTGAAA CCAGCCTGGC CAACATGGTG 360 GAACCCCGTC TCTACTAAAA GTACAAAAAA ATTAGCTGGG CATGGTGGCG AACGCTTGTA 420 ATCCCAGCTA CTTAGGAGGC TGAGACAGGA GAATTGCTTG AACCTGGGAA GTGGAGGTTT 480 CAGTGAGCTG AGATTGCGCC ACTGCACTCC AGCCTGGGTG ACAGAGTGAG ACTGTTTCAA 540 AAAAAAAAAA AAAAAGACAT GCCTCTTCGG TTTCCATATG GTTCAGGGTC AGCCAATCAA 600 GGCAGTTGTT CTGGTCTGGT TCAAGTCCTC AGTGACAGCA AATGCTTCCG GCATTTTGGG 660 TTGAAAGCTG TTGAATCAGT TCAGCCCAGT GAGTTATTGC CAAGTTCCTG TTCTGCGGCA 720 ACCTCAAGCC ATTTGCTGGG GGAGATATGA AAGCCATACA GGCCACCAAA AATACACCTC 780 AGCAGAGCCA GCCCATGGGC AAGGAGCTAC AGTGCGGAGA GATGACACCC GTGTGCAAGA 840 CTGACATAGG TCACAGTAAA GGCAGCCAAT GATTCTGTGT TGCCAAGGGT GGGGATTGTG 900 ATGGTTTAGT CCCTGTGGGC CTTGGTTCTT TTTTTTTTTT TTTTTTTTTT TTGAGACGGA 960 GTCTCGCTCT GTCGCCCAGG CTCGAGTGCA GTGGCGCGAT CTCGGCTCAC TGCAAGCTCT 1020 GCCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGTCTCCTG 1060
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