| Tag | Content |
|---|
EnhancerAtlas ID | HS118-16945 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:1856710-1859450 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SNAI2 | MA0745.2 | chr7:1858347-1858357 | AACAGGTGCA | + | 6.02 |
|
| | 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 |
| GH07I001814 | chr7 | 1854077 | 1859436 |
|
Enhancer Sequence | AGCCACACAC GGCCAATGAG CTCATGCCAG GACGCTGGGC ACCGGGGAAA CGTGAACCGC 60
AACTGAGCGA GACACGGAGC CGCCTCGCGC CGACGGCCAC TGAGAGCAAC CACCATGAGC 120
TGCTGGGTCG AGGGGAATCA GACCCTCCGC GTCGCTGGCG GGAGCGTGTG TGGTGCGGCC 180
ACTGCAAACA GCCGGCAGCT CCTCAAAGAG CTGGACGCAG AGTCCATGGG CCCAGCACCC 240
GCCCGGGCGC GCAGCCAGGG GGTCTGAGCG CAGTCCACGC ACAGACCTCG GCACGGGTGT 300
CCACGGCAAC ACGATCCCAT CACCAACAGA TGGAACGCGG AACCAGCCCT CAACCGCCGG 360
AGGGAGACAC AAAACCGGGT TTACCCGTCA ACACCGCTTC GTACAGCCGA ACTCTGATAC 420
ACGCTGCCAC GCGGGCAAAC CCCGAAAACA CGCCCAGCCA GTCACAGAGA CCTGTCGACA 480
CAACTCCGTG CCCAGGGGAT GTCCTGGAGG GGCACGTCAG GGCTCAGGGC CAGTGGAAAT 540
GTGCCACGGT TAGACTGGTC GCGGCTGCGC ACTGAATGTG CCGGGAGGAA CGGAACGGTA 600
GACTAATGGA GCGCTAGACG TGAGGGTGAG CTGCATGTGT GTGCATCGGA GCTCAGGAAA 660
CCGTTTTGGA AAGCGCTCCC TCCGCCCGGC AGCCCTCTGG GAACCCTCCC CAGGAGCCAC 720
AGGGCGGCCT GGCTCCATCC AGCTTGGTCC TGGCAGCTCC CCTGTCCACC GGAGCATGCC 780
TGGGCTGGGC CCCGCCCTGA TGGTGTCGCC CCTCCCCTCA CCACCTTTGG AGCACGTGCT 840
GCCCCAGAGG CCCTGCGACC TGACCTGTTC CTGCACCTCC TGTTTCTCAG GAGCCGTCCC 900
CGTGCCCTCC CCCTGCCCTC CCCCTGTTTC TGCTGCCTTA GTACATTTGG CCTTGTCATA 960
GTTCAACACA AACCATTTTT AAACAAAAAC AAGAGAAACC ACTCTGACCT TTCGCTGAGA 1020
AAATCCTTTC ACTTCTGCCT TCTGCTCTTG ATTCTGAATT TCTCCCCCTA AATGTCAGAG 1080
GGGCTGATTC TCCTGCAGCT GCCGGGCAGG GGTGGGGAGG CAGTGTGGGA AGAAGTCTCC 1140
TCAGCCGGCC CTTCGCCCTC CTCCCAACCC AGGGCTGGCA ACCTGGCTGG GCCTGACGCA 1200
CTGTGGTGCA GACTCTGGCC AGGCTGGACC AGAGAATAGC TGTTTTCCAG GCACCCGCCT 1260
TCCCCGGCCC TCAGAGGCTG GCAGGCTTTG GGAGCCTGGC CGTTCATTTC TAAAAATATT 1320
TTTTTTTAGA GACGAGTCTC ACTCTGTCAC CCAGGCTGGA GTGCAGTGGC ATGATAACGG 1380
GTCACTCAGC CTCGAGCTCC CGGACTCAAG TGATCCACCT CAGCCTCCTG AGCAGTTGGA 1440
ATGACAGGCA TGTGCCAGCA CACCTGGCTA ATTTTTAAAT TTTTTTGAGA GATAGATAGA 1500
CTTTAGCTAT TTTGCCCAGG CTGGTCTCAA ACTCCTGGCC TGGCTGGTCT CAAACTCCTG 1560
GCCTGACGTG ATCCTCCTGC CTCAGCTGCC CACGACGTGA GGATTACAGG CGTGAGCTCT 1620
GATCATTCTT TATTTGAAAC AGGTGCACCC CGCCAGCGTC AGCAAGACAG CTGCTCCCAA 1680
TGGTAGGCCG GGCAACCCAC TCACGGCTCC TACAGCACCT CCTCTCTGCC GGCCTCAGGC 1740
GGCTCTGGAA GAATGATGCC CTAATATACC GCGCTGCCCT CCAGGTGGGG GTGGGGGTGG 1800
ACGGAGACAG GCAGGAGTAA CCAGTGCTAC TCTCCCAGCT CAAACCCCAC ACGAAGGCAG 1860
ACCCAGCGTT TGCAAAACAC CAGCCCCCGG TGAACAAGTC GACCTGCTGT GCAGCCCACC 1920
TCTGACTCCG TTTCCCCCAG CGTACCCAGC CACATTGGGA GGCTCCACCT CGGTCTAACG 1980
CTCCGGCATT AGCAGGACCT GCTGAATGAG TGGCGCCGGG CCCATCCATC TCTGCCATCG 2040
CTGCTCAGCC CTCTGCCATG TTCAAATATC ACACAGTCCC CAGGTACCTC GTAAATCACT 2100
GTAATTACGG GCTGCTCACT TAAAATTAAA CTGCAATTTT TTAAAAAGCA AATTGCCAGT 2160
AAGACACGTT GGCTGTGGCT GGAAATACTT CTGAGGCTGC CTGCGCGCAG GCTCTGGCTT 2220
CCTCTCCCTC TGCCTGGCCG GCCCGAGCTG CCACCTGTCT AGTCTGCGCA CATAGCGGCC 2280
CTGTGGCTGG CGGGCGCCCT GGGGGAGACT GAGACACTCA CTCTTAATGA AGACACTCGC 2340
GGCGTCCATT GTGGCCACTG CACTCTAGTC CAGACCCTCG CTGGCCTGGC CTGGGGCTCA 2400
CCTGCCCCTC TGGAAGCAGA GAGGGCCTGC CCTGGAGGGC CGGGGACCTC TGCAGCATGT 2460
CCGTGGAACA CGTGGGCCAG GGATTGTGTG CCCGGCCCCC ATTCCAGCTC TGCCACGTGA 2520
GCAGTGCTCA CTCGGTGCCT AGGGCTGACT AGTCTTACTA AGCGCTGGTC CCACCATCCC 2580
CTGAGCCGAG CCCCATGGTG TCCCAGCGGG CACGGACAAG AGGCACGGAG TGAGGGAGGG 2640
GTGGGGGCTG ACAAAGGGCT TGGAGAGCAG AGACAGCGCA CACCACCAAC TCTCTCCACA 2700
CACCACTTTC TCCACACACC ACCAACCGCA GGATGTGGTG 2740
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