| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10593 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:169834180-169836020 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:169835231-169835243 | GTTTGTTTGTTT | + | 6.32 | | JUN(var.2) | MA0489.1 | chr2:169835028-169835042 | ATGAGTCACTTCCT | - | 7.12 | | Mecom | MA0029.1 | chr2:169835973-169835987 | TATTGTCTTATCTT | - | 6.59 | | ZNF263 | MA0528.1 | chr2:169835793-169835814 | TTCCCACGCCCCACCTCCTCC | - | 6.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GATTCATAGT TCCAAATGGC TGGGGAGGCC TCAGGAAACT TACAACCATG GTTGAAGGCA 60
AAGGGGAAGC AAAGCATGTC TTACATGGTG GCAGGAGAGA GCGCATAGGG GAAACTGCCA 120
CTTTAAAACC GTCAGATCTC ATGAGAACTC CCTCACTATC ACAAGAACAG CATGGGGGAA 180
AATGCTCCTG TGATCCAATG ACTTCCCACC AGGTCTGTCC CTCGACACAT GGGGATTACA 240
GTTCAAGATA AGATTTGGGT GGGGACATAA AGCCAAACCA TATCAATCAC TTTAGCTCTA 300
TTGAGGAGTA TAATGTAATC TACCTCCTTA CTGGGTTGCT AATAAAGGTA AGAAATAATT 360
TTTAAATGCC TTAATTTTTT AGTTTCAGGG CACTTTTAGA GTCATCATCT TATTTGAGCA 420
TATAACAATC TTAAGAAAGA GGTAGAATTT GAATAAATTG ACTTTTTTTT TTTTTTTTTT 480
TTTTTTTTTT TCAGAGACAG GGTTTCACTC TGTCACCCAG GCCAGAGTGC AGTAGTGTGA 540
TCATAGCTCA CTGCATCTTC AAACTCCTGG GCTTAGGCCA TCCTCCCATA TCAGCCTCCT 600
GACTAGCTGG GACTATAGGC ATGTGCCACC ACACCCGGCT ACTTTTTAAA TTTTTTGTAG 660
AGACAGGGTT GCCCAGGCTT GTCTCAAACT CCTGGGCTCA AGCTATCCTC CCGACTTGGC 720
CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACCATGCC TGGCCATCAA TGAACATTTT 780
TATGTGGTTT TTAACAATCT CTCTGTACTC CAATATATGA AACCCCAAAT TATAAAACAG 840
ATAAAGCAAT GAGTCACTTC CTTAATAGGT TACAACTTCA CTGTTTGGCG AAAGAGTATC 900
AAACAGCGGA CAGTGAACCA AACAGGTTCA GGGAGCCCGC AAATCACCTC TGGATTTCCA 960
GGGCTTGCTT TGGACTCAGC TCAGGGCATT TTTTTTTTTT AAAGAGAAAG AACAACAGAT 1020
TGCCAACTTC CCCTTCTGTT CTTGGTTTTC TGTTTGTTTG TTTTTTGAGA CACGTTCTCA 1080
CTCTGTTGCC CAGGCTGGAG AGCAGTGGCG CAATCATGGC TCACTGCAGC CTCGGCCACC 1140
CTGGGCTCAG GTGATCCTCC CACCTCAGCC TCTTGAATAG CTGGGACTAC AGGCACATGC 1200
CATCTTGACT GGCTAATTTT TGTGTTCTTA GTAGAGACAG GTTTTCACCA TGTTTCCCAG 1260
GCTGGTCTTG AACTCCTGGG CTCAGGTGAC GCGCCCACCT TGGCCTCCCA AAGTATTGGG 1320
ATTACAGGCA AGAGCCACCA TGCCTGGCCT GTTCTTGGAT TTTGACTCCC TAGCTTGGCC 1380
TCCAGTGTGC TTCCATAGAC TAACCAGTAA AATCCCTTTT TGCCATATTT AGAAGATAAG 1440
CGAATTTTAT GGACATGGTC TTGAAGTCCT GCATGGTAGG CCCTTCCCAT GCCTCCAGCC 1500
TCTGCCCCTT GTTCACTCTA TTCAGTTGCA CTGGGCTTGT TTCAGCTTCT TTAAATCAGC 1560
AGCCTTTTCC AACTTGGGGG CCTCTCTTCC ATGAATGCCC TCCCTGCTCT TACTTCCCAC 1620
GCCCCACCTC CTCCAATCCT CATTTGTATG GCTGACTTTT CTTCAGTTCT CCACTCAAAT 1680
GCTACCTCCT CAGAGATACT GCCACCACCA CCCAATTTAA AGACTCTTTC TCCCACCCCA 1740
GTCGCTGTCA CATTGCCCTA TTTTATTTCC TTTATTTACT TACCACTCTC TGCTATTGTC 1800
TTATCTTTGA ATGTGCATAC TTCTTTACTG CCTGTCCTCT 1840
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