| Tag | Content |
|---|
EnhancerAtlas ID | HS118-03190 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr11:14223650-14225870 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DMRT3 | MA0610.1 | chr11:14225386-14225397 | ATTGATACATT | - | 6.62 | | IRF1 | MA0050.2 | chr11:14224199-14224220 | AGCTTCTTTCACTTTCAATCA | + | 6.22 | | ZNF263 | MA0528.1 | chr11:14224645-14224666 | CCCTCCTCTAATTCCTCCTTA | - | 6.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAATTGAGAG CTCTAATTGA ACACTGTGGG AACCAAGCAT GAGTCAAAGA CATCGTCCCT 60
TTACAAGTGG CAGTCACCGA GGAAACGTTC ACTTGTGTGT CAGAGGGACA CCTAACATCA 120
GCAAGAGTAA CAGTAGCTGA GGCTGAATGA AGGCTTGCTG TGTTGGGTAC GCATGTCAAG 180
GGAGACGCAG GACGCTATTT GCCTCACATC TCCCTCATCT TGCAGTCATC GCCGTCCTGT 240
GCCTTGGTGG AGTTTTTAGT GTATGCAGCT TCTGTGAACA CAAGGACCTC CCCATCATGT 300
CCATTGCACT CCCTCCATAC CTAGCACAAG TGCATGGTCC GGAGTAGTGC CCAGTGAATA 360
TGTGTCAGGA CAGTGGGGAA GGGAGGAGGA CAATACCCTC TAACGGCCCC AGAGTCTGTG 420
CCTTCTGGCC CAGATTCAGT CAGACTCCAC CAAAGTCAGT CTCCAGGACT CTGTTTTCCA 480
AGTTTGTTCA GCCCTTCCCC CTCAGCTAAC CTGTTCGTCC CTTTGAGCCA AACTCACTGA 540
TTAGCATTCA GCTTCTTTCA CTTTCAATCA TGCCAGACCC GGTGTTTCAT GCTTAACCGT 600
TAGGGAAACA TCCTGTCTTT TACCATGATT TTTGCAGGTG GCTAATATCA TCAATTATTT 660
TACTCACTCA ACTCTCAGAG GGTAATCACT TCTTTGATTC AAGTTTCAAG GCCATCTCAC 720
TGTGGGCTCC TATACATCAC CGATTACACC GGGCAGAGTC AAGCAGAGGT GCTGGCCCTG 780
TTCTTTACAG ATTCATCTGG AAACTATGGT GCTGTTAATC TGCTCTGTGT TCATGCTAAT 840
AGTGTCTGTC TATAATCAAC CTCAATCTAC CATTCACCAC GCCAAAAAGA TAAATGCCAG 900
ACTTCAGAAA ATGAACTAAA GGCAGCCCTC AAACCCCAGA AAATCTCCTG TCCACCCCTG 960
CCAGGGCGCA AGATGTCCTG ATTTAGGAGG TTGATCCCTC CTCTAATTCC TCCTTAGAAT 1020
GTATTTCAAA ATCAAAAGCC AATAGTTACA TTTCTAAGCA ACGGAGCAGA CCAAAAATGT 1080
TTTGTTTGAC ACAGAAGCAA TAGAAGCAAG ACCATGTTTC TATTTTATGA AACCTCTGAG 1140
GGTAATTCAC TGAAATCTTG ACATTTAATA TCACCCAATC ACCTCTCTAG CAAGCTATTT 1200
TCTTTGGCTC CATTAACCCC ACACACACAG ACTGGGCTGC TGGCACTTAC TGGGTCTTGT 1260
CGTTAGGTGG GCTGCTTTTA ATACCAGGGC AGGATTTGGC AGGAAGAAGT GGCACCTGCT 1320
TTATTGAAAG ACATCTTCAT ATTTTAGCCT CTGAAAGAGA AATGTGCAAC ATAAATGTCC 1380
TTAAGAGACG ATTATCGTAC ATCAAGATGT CCATTCCAAA AGGCATTGTA CCAGATGCCC 1440
AATCACACAC AGTCACCCAG AACAGACGTG ACAGATGGAG ACTTTGAGCT TTTAAAGAAA 1500
ACAAATGTGC AAATTCCAAA GTGTCTGTGT GCTCCAGGCC AGCACATGCC CAGGTAATTT 1560
GAGTTGTGCC CATTGGCTGA AAGATAAGAT TCAGGCCTCA GAGAGGGTTT GGGGAGAGGA 1620
TGAGTACAGG TTTCTTGTTG CCCAGAGTCT CCAAATAGAT ACACACAGGA TACACCACCT 1680
CAGCCCAGAG ATATTTAAGC ACTGAGTTAA AAGAAAGGAT TGAGCATGCA GCATCAATTG 1740
ATACATTAAT GCTGGTTCTC TGGCATCAGG GAAGACATTA ACATACAGAA CTTGTCTTCT 1800
CCACTGTTCA AAAATGGGAA GAATCATTCC AACAGGGAGA GCAGGGAAGT CCAAAATCCA 1860
TAATGCTCAG GTACAAAGTA ATGAAACCAG AAATCCAGGG TATTTTTGCT ATTACTACCA 1920
AGGGCCTATC TTCGGTGTAA TGGCAATCTT CTAAATCTCT GCATAGTTTG ACACCTGCAA 1980
ATCTGATTGA GTCTGATTGA ACCATTTGCT GTCTAAAATC CTTGGGAGAC CCCGATAACC 2040
TAGAGCTGTA GCTTTCAAAT TGCTCCATGG GCTCGGGCCA AGGCTTCCAC AGGGACTGAG 2100
GGAGGAAGGG TACAGCTCTT GGGCACATCC CCTTGGCTCC AGTCAGAAAA GTTATTTCCT 2160
CTGTTTTACA AATTGAGCTT CCAAGTAAGA TTTTCTTCTT TTCTCTTTTT ATCTGTCTCT 2220
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