| Tag | Content |
|---|
EnhancerAtlas ID | HS091-40877 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr6:34157080-34158920 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:34158690-34158709 | TACCACCACCTGCTGGAAG | - | 6.04 |
|
| | 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 |
| GH06I034189 | chr6 | 34157671 | 34158488 |
|
Enhancer Sequence | GGAGGCGGAG CTTGCAGTGA GCCAAGATCA TGACACTGCA CTCCAGCCTG GGCGACAGAG 60
CAAGACTCCG TCTAAAAAAA AAAAAAAAAA ACTTTCCATA CATTTGAGAA TTTAAAACAC 120
AATGTTTCAA AATAAATCCG GTCTGGGAAT TGGAGGAGTA TATGGGAATA TAGATTTTAA 180
AAAGACTGGC CATGTTAATA ATGCTGCTGA ACCTGGCTAA CAGGTACCCA CTGCGGTTCA 240
TTATATAATC TCTTATCTTT TATATATTTC CTTTTTTCCA TAACAAAAAG CTTTTTAAGC 300
ATGGTAGTGT GCACCTATAA TCCCAGCACT TTGGGAGGCT GAAGTGGGAG AATCATTTGA 360
GCCCAGGAGT TCAAGATCAG GCTGGGCAAC ATAGCTAGTC TCCATCTCTA AAGAAATTAA 420
ACAGGCCCTC GGCAAAACCT GAGTCCTGTC CTCTCGCTTT CTTCCCTGGA CAGCATGAGC 480
TTCACCACTC GCTCTACCAC CTTCTCCACC AACTACCAGT CCCTGGACTC AATGCAGCCG 540
CCCAGGTACA GCGCCCAGCT GGTCAGCGGC ACAGCCAGCG TCTATGCAGA TGCTGAGGGC 600
CCAGGCTCTC AGAGGGCCCA GGCTCTCAGA TCTCTGTGTC CCACTCCACC AGCTTCCAGG 660
GTGCCTTGGG GTCTGGAGGC TTGGCCACAT GGATGGCCAG GGGTCTGGCT GAAATGGGGG 720
ACATCTAGAA CCAGAAGGAG ACCAATCAAG GCTTGAACGG CTGCCTGGCC TCCTACCTGG 780
ATAGAGTGAG GAGCCTGGAG ACTGAGAATC GGAGGCTGGA GAGCAAAATC CAGGAGTATC 840
TGGAGAAGAA GGGACCCCAG GTCAGAGATT GGGGGCATTA CTTCAAGACC ATGGAGGACC 900
TGAGGGCTCA GATCTTCGCA AATTCTGTGA ACAATGCCAG CATCATTCTG CAGATTGACA 960
ATCCCCATCT TGCCGCTGAT GAGACAGAGC TGGCCATGTG CCAGTCTGGA GAGCGACATC 1020
TGTAGGCTCT GCTAGGTCAA AGATGACACC AATGTCACTC GGTTGCAGCT GGAGACAGAG 1080
ATCAAGGTTT TCGAGGAGGA ACTGCTCTTC ATGAAGAAGA ATAACATGAG GAAGTTAAAG 1140
GCCAACAAGC CCTAATTGCC AGCTCTGGGT TAACCGTGGA GGTAGATGCC CCCAAATCAC 1200
AGGATCTTGC CAAGATCATG GCAGACATCC AGGCCCAATA TGACAAGCTG TCTCAGAAGA 1260
ATCGAGAGAA GCTGAACCAG TACTGCTCCC ACCAGACTGA GGAGAGCACC ACAGTGGTCA 1320
CCACGCAGTC TGCCAAGATC AGAGCTGCTG AGATGACGCT CATGAAGCTG AGACGTACAG 1380
TCCAGTCCTT GGAGATCAAC CTGGACTCAG TGAGAAATCT GAAGGCCAGC TTGGAGAACA 1440
GCCTGAGGGA GGCGAAGGCC CACTACGCCC TGCAGATGGA GTAGCCCAGT GGGGTCCTGC 1500
TGCACCTGGA GTTGGAGCTG GCACAGACCC GGGCAGAGGA GCAGCGCCAG GCCCAGGAGT 1560
ACAAGGCCCT GCTGAATATC CAGGTCAAGC TGGAGGCCGA GATGGCCACC TACCACCACC 1620
TGCTGGAAGA CGGCAAGGAC TTCAATCTTG GGATGCCCTG GACAGCAGCA ATTCCATGCA 1680
AACGACCACC ATCCAACAGA CCACCCTCCC CCCGCCGCCA GGATAGTGGA TGGCAAAGTG 1740
GTGTACGAGA CTAACAACAC CAAAGTTCAG AGGCATTGAG CCAGCAGAAG CAGGGTACCC 1800
TTTGGGGAGC AGAAGGCCAA TAAAAAGTTC CAAGGTCATT 1840
|
