| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01046 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:120263940-120265130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESX1 | MA0644.1 | chr1:120264709-120264719 | GTTAATTGGT | - | 6.02 | | IRF1 | MA0050.2 | chr1:120264460-120264481 | CACTAGTTTCTCTTTCAGTGC | + | 6.09 | | NR2C2 | MA0504.1 | chr1:120264531-120264546 | CAGGGGCAGAGGTCA | + | 6.72 | | Nr2f6(var.2) | MA0728.1 | chr1:120264706-120264721 | GAGGTTAATTGGTCA | + | 6.02 | | RARA | MA0729.1 | chr1:120264652-120264670 | CATTGTCCTTAAGACCTT | - | 6.32 |
|
| | 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 |
| GH01I119720 | chr1 | 120263376 | 120266116 |
|
Enhancer Sequence | TGAAGTAAGT CATGGAGGCT GCGGGCGGTT TGGGGGTAGG GGGGTGAGTG CGGAGACTGA 60
CCACACCTAG GGAGAAAAAA CTCACTTGAG AGAAAGCTGA GTCCATTGGA AGGGCTTCCA 120
GGAGGATGCC TGGTCTAGGG CCTGCATGGT CAACACACAC AGCATAGTGG TTTCAAGGTT 180
TTTGGAAGGC AGCTATGCTC ACCACTATAT CACCAATGCC ATCAGGGTGT TACACAGTTT 240
TTGAAATTGA GAGTCCCTGC ATAATCTCAA AATGTTTCAC GAGCCCACCC CATGCGCAGT 300
TGCTTGCACC TCTGTGACCT GGTTCAGGAA TCGGAAGGTC AGTGAGTTCA TCTGCATTTC 360
CTGCTCCCAC CCAGCCCCCT CTGCCTCTAT TAATGCTGTT TGTGGCAGGT TTTTGTCAGC 420
TCTACTTTAC TGTGCTTGTA CAGAGGCACA ACCTTTGCTA GCAGACTAAT GACTAGAATC 480
CTTGCCCTCC CCACTTCCCT GCCACCTTCT GGAACTAAGA CACTAGTTTC TCTTTCAGTG 540
CTCTAGGGCA AGAGGAGAAG GGTCCCATTT AAAGCTGTTT CTGCAGAAAC ACAGGGGCAG 600
AGGTCATCAG CACGCCAGTG CTGTACTGTA CCCGTTCTGT CACTTAGATG GTATGGCAAG 660
GCCATCCCCA GGCCTCTTTG TTCTTAAGAC TTTTCTCTTC CCTTGGGGAC TTCATTGTCC 720
TTAAGACCTT TCCCCTCCCC TGCACTGCAC TTCCCCCTGT AGGGTAGAGG TTAATTGGTC 780
ACCTGACTGA AGTCAATATT CAACAGCAGA AATGTTAAAC GATAACCCAT CCCACATTCT 840
TGCCTTGGAC CCAGAGGCAG CCAGGCCCCA ATCTCTGCAC CTCTACTTGC GCCCCCATAC 900
AGCCTGTTTG CTGTGGGAGG ATGAGAAGCC AGGTGGTTTT GCAGGCAGAC AGACTCTGAG 960
AGTCCGTTTA TCTTATACAG GATCTCTTGA CTTTTTCTTC TTGTAACCTT ATTAACCTTC 1020
ATTCCAGAGA TGAAAAAGAC AGACCCAGTA GGGGAATAAT CAGGGTGAAC ACGTATATGA 1080
AATTCTTTCA AAAACCTAAA AAGCATTTAA GAAAAGAAAA ATAGTTTTGT GGGTTGCCAC 1140
CTCTATTTTT TTGTTTATAA AATGGGAAGG GTCTGGATTG CCCTGTGACT 1190
|
