| Tag | Content |
|---|
EnhancerAtlas ID | HS060-13990 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr17:4919540-4920760 | 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 |
| | | 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 |
| GH17I005016 | chr17 | 4919691 | 4920772 |
| Enhancer Sequence | TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC TACAGGTGTG CGCCACCACA CCCGGCTAAT 60
TTTGTATTTT TAGTAGAAAC AGGGTTTCTC CAACTCCCAA CCTCAGGTGA TCCTCCTGCC 120
TTGACCTCCC AAGGTGCTGG GATTACAGGC TTGAGCCACC ACACCCAGCC CTAATTTTTG 180
TATTTTTAGT AGAGACAGGG TTTCACCATG TTGGTCAGGC TAGTCTTGAA CTCCTGACCT 240
TGTGATCCAC CTGCCTCGGC CTCCCAAAGT GCCAGGATTA CAGGCGTGAG CCACCGCACC 300
CGGCCAGCAC ATTTTAAAAA ATAACAAAAG ACGCTATCAT GTGCGTCTTA CAGTGAGGTT 360
TAAGACATAC CTCTTGGGGC TGGTGGGGTG GCTCATGCCT GTAATCTTAG CACTTTGGGA 420
GGCCGAGGTG GGTGGATCAC TTGAGGTCAG GAGTTTGAAA CCAGCCTGGC CAACATGGTG 480
GAACCCCGTC TCTACTAAAA GTACAAAAAA ATTAGCTGGG CATGGTGGCG AACGCTTGTA 540
ATCCCAGCTA CTTAGGAGGC TGAGACAGGA GAATTGCTTG AACCTGGGAA GTGGAGGTTT 600
CAGTGAGCTG AGATTGCGCC ACTGCACTCC AGCCTGGGTG ACAGAGTGAG ACTGTTTCAA 660
AAAAAAAAAA AAAAAGACAT GCCTCTTCGG TTTCCATATG GTTCAGGGTC AGCCAATCAA 720
GGCAGTTGTT CTGGTCTGGT TCAAGTCCTC AGTGACAGCA AATGCTTCCG GCATTTTGGG 780
TTGAAAGCTG TTGAATCAGT TCAGCCCAGT GAGTTATTGC CAAGTTCCTG TTCTGCGGCA 840
ACCTCAAGCC ATTTGCTGGG GGAGATATGA AAGCCATACA GGCCACCAAA AATACACCTC 900
AGCAGAGCCA GCCCATGGGC AAGGAGCTAC AGTGCGGAGA GATGACACCC GTGTGCAAGA 960
CTGACATAGG TCACAGTAAA GGCAGCCAAT GATTCTGTGT TGCCAAGGGT GGGGATTGTG 1020
ATGGTTTAGT CCCTGTGGGC CTTGGTTCTT TTTTTTTTTT TTTTTTTTTT TTGAGACGGA 1080
GTCTCGCTCT GTCGCCCAGG CTCGAGTGCA GTGGCGCGAT CTCGGCTCAC TGCAAGCTCT 1140
GCCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGTCTCCTG AGTAGCTGGG ACTACAGGCG 1200
CCCCCCCACC ACCACACCCG 1220
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