| Tag | Content |
|---|
EnhancerAtlas ID | HS091-12293 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr13:113793780-113795230 |
Target genes | |
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 | chr13:113794235-113794246 | TTTGATACATT | - | 6.02 | | Foxo1 | MA0480.1 | chr13:113794072-113794083 | TGTAAACAGGA | - | 6.62 | | Myod1 | MA0499.1 | chr13:113795193-113795206 | TCCAGCTGTCCCC | + | 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 |
| GH13I113138 | chr13 | 113793233 | 113794043 |
|
Enhancer Sequence | TTATGTAGGT TCCTCTGCTT GGTATACCTT CAGATCAGAT GCCCCTGAAG AGTGGCAGGT 60
GGGCGGGGGA AGAAGTGAAA ACGCCTAATG AAACAATCTT AAGTCATTTC TGATTTACAA 120
AGTCTGGGCT CTATTATACC TATTATACTG TGCCACTATA GCAATAGAAA AAAAAGCCCC 180
AATATGTCCC CCAAACGATT CGGTTTGGGG GCATGATGAG AGAGACACAG TCACTTCTCT 240
GCTCCTCCGA GAGAGACTGT AGAACATTGA TGAAGCGTGT GATCCATTCA TGTGTAAACA 300
GGAGTGGACT CTCTGTTTTC CTTGGGGCCA AGTGCATTGC CCTGTTATTC CTGCTCCTTG 360
TGACCCTGTG CAGTGATTCT AAATCACCTC TTATTTATGT GTATGGATGC AGGTGTCAAT 420
ATTTGTGAAT ATTTGTGATT GGCCAATTAT AAAAATTTGA TACATTTAAT TAGTTCTACG 480
TGGAAAAATC ACTAAGTGCT TTCTCTAATG TGGTGATTAA GTTTTAAATA AAAAGTTAGG 540
CTACTGTTAG ATCAATTTCC CTAAGGAAAA AGATTTGCAT TTCTTTTAAA GTACTTAATT 600
GATCATCTTT TTTTTTTTTT TTTTTGAGAT GGAGTCTCGC TCTGTGGCCC AGGCTAGAGT 660
GCAGTGGCAC GATCTCAGCT CACCGCAAGC TCCGCCTGCC AGGTTCACGC CATTCTCCTG 720
CCTCAGCCTC CCAAGTAGCT GGGACTATAG GCCCCGGCCA CCAGTCCCGG CTAATTTTTT 780
TTTTTTTTAA TTTTTTAGTG GAGACGGGGT TTCACCGTGT TAGCCAGGAT GGTCTCGATC 840
TCCTGACCTG GTGATCCGCC CGCTTCGACC TCCCAAAGTG CTGGGATTAC AGGCGTGAGG 900
CACAGCGCCG GCCTAATTGA TCATCTTTAG ACTGTGTTCT TAGATTGGAT TACTTTTGAG 960
TTTTCCCTGA TGAGAATATC AATTACGCAT CATTCCATTC CAAGTCCGCA GTCGCCTCCC 1020
TGGAACACCA TTTGGTAACT TATGAGGCAT AACCCTGTTC AGGCTCCCAG GGCTATTATG 1080
CACATTTTCT AAAATTTCAG GCATGTTGAT CTTTGCACTG TGATTACTTT TTCATCAAAA 1140
GCCACACAGA GGGATGTGGA GTGACCGTAA TGTGAGTGCT GCTGGGGCAG GGGGTACCGG 1200
CCATCCCGGA GGTGTGAGGG GCAGGTACCT GGAGCCTGGC TTCTGGCTAC ACCGGGCACT 1260
GCACCATGAG CTCCCCGTGA CCCGTGAGGT TGCCCTTCAA GGCAAGTGTA CCTGTCGCCT 1320
GGCTCTGGCC CTTTGCTCAA CCCAATGGCC GCTTTGTGGC TGACAGGCAA GTGGATGTAG 1380
CTGGCACCCT TGGGCCAGCC CAGCCTCCAT TTCTCCAGCT GTCCCCAGAG CCAACGTGCC 1440
TCTCCTTTGC 1450
|
