| Tag | Content |
|---|
EnhancerAtlas ID | HS118-07686 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr17:81900-83800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr17:82469-82481 | GATTGTTTATTT | + | 6.62 | | HNF4G | MA0484.1 | chr17:83377-83392 | CAGGTGCAAAGGTCA | + | 6.15 | | IRF1 | MA0050.2 | chr17:83510-83531 | GAACGGTTTCACTTTCTTCTT | + | 6.51 | | Nr2f6(var.2) | MA0728.1 | chr17:83305-83320 | AGGGTCAAGGGGTCA | + | 6.3 | | RARA(var.2) | MA0730.1 | chr17:82023-82040 | TGACCTCTCCATGACTT | - | 6.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 82080 | 82131 | | chr17 | 82268 | 82382 | | chr17 | 82497 | 83686 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I000232 | chr17 | 82392 | 84990 |
|
Enhancer Sequence | AAACACCCGC CAAGCAAGAC GTGGCCGGGC CTCTACTCCC CTGAGATTTA GGGAAAGGGC 60
AGTTTCCTGA CTGCTGCAGG TGTTTCTCTG CCTTTCCATG CTGAGACTAC GGTGCAAATT 120
ATTTGACCTC TCCATGACTT AGTTTCCTAT TCTGTAAAAT GGGACAACAG TAGCGGCCCC 180
GTCACAGGTT GTTGGGGGAT GACACGAAAT AACGGAGACG CACAGCGCCC AGGACAGCCT 240
GCAATGAGCA CCCGTGTCAT CTATGGCAGC TACAGCTGTT GCTGTTTTTA TCGGACTCCT 300
CAGCACCAAG GGCCAAAGCC CATCCCTTTT ACCTGCACAG ACAGACAGGC AAATGGTACC 360
CAGGCCTCGG CTGACCCTGG CAGAATGGCA GCTGCCTGAG AAGACCAAGG CCGACTATCA 420
GTGTCTCTCC CAGCGGGACC CACGGTGGCC TCGGGCAGTG CAGCGTCACC CCCCTCCCCT 480
CGCCCTGTCT CAGCTGGGAG GGATGACATT CATTCCCCAA GTGTCTGGCT GGACCAGAGC 540
CACAGACACA ACTGTCTATG ACATTGTTTG ATTGTTTATT TTCTTGACCC AAACAGCAGA 600
CCTGCACCAG GGAGATCTGA GTCAGTGGCT TCCAAGGTGC CACACAGGGC CTGTGGTGCC 660
GTTCTCAGGT GGTTCAAAGA CAACTCCCCC CTTCCTTGTC TCTAAACAGT CCTTTCCGGC 720
GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTTG 780
GCTTCTATTA GCTTTACATT TCAAAAATCC CAGGTACTTC CAGCTCCCTG GGACTACAGA 840
ATCCATGCAG GGAGGAAAAT GAACAGAGAT GGGGAAGGTG ATAATTAAGC ATAAGAGGCC 900
TTCCTGGGGC TAGGACTTGG GAAGGAAGCT TCAGTCAGTT CATGGCACTT AGTGAGCGCT 960
TATCAAAGCA TAGTGGGGAT GCTGGGTGGG TCTGACGGGA TTTCGTTTGA CAGCATGTGC 1020
CTGTCTGTGT GGCACGTGTG CGTGTGTGTG CAGAGGGTGG GGCCAACATG GAAATGGGGC 1080
TGGGCTTTCC AGTAGAGCCT GATCTGAGAG CTGCCTTACC AGCCACTGCT CTACCCCCCG 1140
CCTGAAATTC CTCTGTAAGT TTCATTCCCT TGGATTTAGA CCTGTAAGAC ACGACCGCTG 1200
GGAGAGAACA GACTCTGTCC CAGCCCCTCA TCCATTCTAC TCATGGGGAA ACCAACACCT 1260
AGAGAGGAAA AATGACTTCC AACGCCAAGA CTGTCCGGCC CAGGAGTCCC CCAGGAAAAC 1320
ACCAGCCCTG TGGGGGCTGG GCCTGTAAGC CCTGCTGATG AGGTCACGTT GGGCCACCTC 1380
CATGATCATG GCAGCCACTA GGGGCAGGGT CAAGGGGTCA GGGTTAGGAG TACAGTCACA 1440
CAGACGTGAC CTGGTCATGC CCCTGCCTCC CACTGGCCAG GTGCAAAGGT CAGGGAGTGA 1500
AGTGAGCTGG ACATGAGGGC CCTTCCCTTC TGAGAGAAGC ATGCCCATTT TTCTTGCAAC 1560
AGGCACCCCT ATTGGTCTGT CTTCTTTCTT TTCACAGGGA TGTGAAACAA GAACGGTTTC 1620
ACTTTCTTCT TAAAAACACT GCAACGGTGA TGCTGAAAGG GTGTCAGAGA CAACAGGGCC 1680
GGGTGGGGAC TGCAGCGAAC CACAGAATGC AACCGGGGAG CGGCTACTTC CCCTGACCAA 1740
CTTCCCTGAG CAGGGAGCGG CTACTTCCCC TGACCAACTT TCCCCCAAGC GGGGAGCGGC 1800
TACTTACCCT GACCAACTTC CCTGAGCAGG GAGCGGCTAC TTACCCTGAC CAACTTCCCC 1860
GAGCAGGGAG CGGCTACTTA CCCTGACCAA CTTCCCCGAG 1900
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