| Tag | Content |
|---|
EnhancerAtlas ID | HS053-19116 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr19:9956980-9958700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr19:9957141-9957158 | CAGGTCGTGGTGACATC | - | 6.02 | | ESR1 | MA0112.3 | chr19:9957524-9957541 | TGTGTCAGGGTGACCTT | + | 6.36 | | ESR2 | MA0258.2 | chr19:9957525-9957540 | GTGTCAGGGTGACCT | - | 6.5 | | PPARG | MA0066.1 | chr19:9957522-9957542 | AGTGTGTCAGGGTGACCTTC | - | 6.19 |
|
| | 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 |
| GH19I009846 | chr19 | 9956928 | 9958725 |
|
Enhancer Sequence | TAGAGGCTGC GTCATCCCTG GGATGCAGTC CCCATGGAGG GGAAGAATGA TGACAGCAAG 60
GGACGTTGGT CAGGGTCCTG CTCGGTGCCG GGCACTATGC TGCATGTCAC AGCCACTGGC 120
ACAAGACTGT CAGGCGGAGG GGCACAGGGA TGTCAGGGCA GCAGGTCGTG GTGACATCCA 180
GCTCAGATAC CAGGACACTG GTGGCTGCCA TGACGTGCAG CCAAACAGGG AGCTATGGCT 240
GTGCTCTCAC GGTGGTACCA TTTCCACTGC AGTCCCAAGC AGGTTAGAGC GTGAGGCCGA 300
GGGGCCCTGG GGACACTTGG ATCAGTCCAG TGTGTTCAGC AGGTGCCACG GTTGGGTGTC 360
CAGGCCTCCC AGCACTGGCT AGGTCACCCA GCAGTGTTCC CGTGGGTCTC CAACAGGCTC 420
CAGGCCAGTG TATCAGCTAT GTATGTCCTG GGCAAGTTGG CCGGCAGGTG TGTCATGGCA 480
TCATTTAGGT CAGAAGGAGC AAGGGTAGAA GTGTCAGGGT GACATTAAGA AACCCCCTAC 540
TGAGTGTGTC AGGGTGACCT TCACGTTGGA GAGAAGAACT GGTGTCCCTG GAGAGTGGCT 600
GCCAGGCCTT AGGGTACACG GGGCGGGTGC AGTTCACCCA GAGGGCTGCC CTGGCTTGCT 660
GGGGCTGTCG CACCACTGGC CTAGGGAGGA CACTGGAAGG GACGCCCGTT TGTGTCAGAG 720
CAAGAGGATT GGGGTAGGGC AGGCTTTGGC CCATGGGCAC CTTCCTGGGG GTGGCCTGGA 780
GTCAGGAAGG CGGTAGCCAT TCCTCCTGAC CTGGCACGTG CACAAGACTG CATACACACA 840
CTTGCTCACA CACAGTCACA CCACACACAC CACGTGCACA CACACGCAGC CCTCCCCACT 900
TGGCTTCCGA AACGTGAGTC ACTCAGATGC TACTCTGCTG CCGTCTTGCC CCCTCTGCTG 960
GCAGCCCTGT TCCTCCTAAC TCCACCAGCC CTGGCCTCCT CCGCCTCCTG GAGAGTCAGA 1020
GCCGATGGGC TAGTTTGGGC CACACAGGGT GGGGCCACCC TGAGTTCTGC CAGCATGCAG 1080
ACTGTAGGTG GGGAGCCGGG AGAAGAGCTA TGTTGCCTGC CTCTGGGACC CTGGGGCTAC 1140
AGCCCACGAG TGTCCCTTGC AGAGCCCACC AGGGTGCCTT GGAGGCCCAT CCCAGTGCCA 1200
GGCTGTTCTT CCCAGATGGG ACAGCTGGGG CCACAGGCTG CCGTGGCAGT GCTGGGCTTT 1260
CTCTGGACAG CTCTCCCACC TCTGCCCAGG GGGCCCGGGG GGCCAGCCCC CTGCCTGGGT 1320
CAGCCTCTCC CTGCCTGCTG CTCTCCTCTG GCCCATCCAG CTTGTATGTA GATTTTCCCT 1380
CACGTGTGTG TGTGTGTGTG CATGTGTGTG TGCTGGTGAG AGTGACAGCG GGAGCAGGGA 1440
TGTGAGACCT GCAGGGTGGC AGGGCTCATG GATGACTGGC GGGGTGCATT AAGTGCTCAT 1500
GCTCGTGAAA GGCACCTCTT CTTGGGTGTG GGTGAGGACA GGTGTGACTG CGCATGCAGG 1560
TATGTGTGAG GAGAGGGGTT GTGGGGAGCA TGTGCGCCTG TGAGGGGAGG CTTTCCAACT 1620
GAAGTGCTGC CTCCCCCGCT GGCCAGCTCT GGAGTCCTCC ATCCTGTCTG GTCAGGCCCC 1680
CCCCAACCCC TGACCTGGCA CTCCCATTCC GTTCCATGTC 1720
|
