Tag | Content |
---|
EnhancerAtlas ID | HS095-12914 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr17:54775320-54777820 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr17:54776336-54776347 | GTCAAGGTCAT | + | 6.32 | Esrrg | MA0643.1 | chr17:54776337-54776347 | TCAAGGTCAT | + | 6.02 | HES2 | MA0616.2 | chr17:54775685-54775695 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr17:54775685-54775695 | GGCACGTGCC | - | 6.02 | RARA(var.2) | MA0730.1 | chr17:54776329-54776346 | AGGCCAAGTCAAGGTCA | + | 6.36 |
|
| 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 |
GH17I056697 | chr17 | 54774751 | 54777998 |
|
Enhancer Sequence | TTTTTTATTT TTTGTAGAAA CAGAGTCTCC CTATGTTGCC CAGGCTGGTC TTGGACTCCT 60 GAGCTCAAGC AATCCTCCTA CCTCAGCCTC CCAAAGTGCC CAGGCCAGAG CACAGTAGTG 120 TGATCTCGAC TTACTGCTTG TGCCTCCTGG GCTCAATTGA TCGTCCCACC TCAGCCTCCC 180 AAAGTGCTGA GATTACAGGC AGGACCCACT GCACCTGGCC AATTTACTCT TTTTTTTTTT 240 TTTTGAGACA GGGTCTCACT CTGTCACCCA GGCCAGAGTA CAGTAGTGCA ATCTCAACTT 300 ACTGCCTCTG CCTCCTGGGC TCAAGTGATC ATCCCACCTC AGCCTTCTGA GTAGCGGAAA 360 GTACAGGCAC GTGCCACCAT GCTTGTCTAA TTTTTGTATT TTTTTAGAGA TGGGGTTTTG 420 TTATGTTGCC TAGACTAAGG TTATTCTTAT ATTCTTTAAA AGAATGAAAT TTTCCATGAA 480 TGTCTACTCT CAGGTATCTC GATGACCACA GACTTTAGAT CTTAGAAGCA TCTTAGAGGA 540 AATCAAGCCT AAATTCTTCT TTATTTTACA AATTAATACA TGTGATTCCG AGACATTAGG 600 GGATTTGCCT GGAGCCATAC AGCTGGTTAA TGGCAGAGCT GAAACTAGAA CAAGGTCTTC 660 TGATTCCAGT GGTGCAGTGG CACCATTGCA AGGTCTTGGA GGAACAATGA TGGTGATGAT 720 GATTCAAGAC CCTACTGTTT GACAGGCATA GTATGACTTA TTTTATACAC ACCACCTTAT 780 TTATTCTTCA CAATAGCCTG GTATAATGGG TACTATTATC CACCCATATA GATGAGGAAA 840 CAGGCTCAGA GAATGAGATA CCTTACTCAA ATTCACACAG CTAGTTGGTA AGGGGGGCCT 900 GGATCCAAAT TCTGTGCTCC TTTGATTTCA CTATGCTCTA TTTCCACCGA GGAAGTGGGT 960 TCCCTGGTGG GGCCAGGGAG GTGGCTCTAT GGCTATGAGC CAAGATTTTA GGCCAAGTCA 1020 AGGTCATGGA CTCTTGGGAT CAGCCCTGGG GCCAACAGGC TGCCAGAAGT GACAGAACGA 1080 AGAAAGGAAA GGAAGGAGAG AAACAGGAGA CAAATCTTGA TGGCTTCCCC ATATTGCCAT 1140 TGTCCTACTT GGGGAGTTCC ACCTTCATCT GTTTTACCCT TTTTTTCCTT TACCTTCGAG 1200 CTCTACGTCT CTTTATCAGT AAACTAGCCT TGCAGACAAG TGCAAACTGT GCCAGCCCTT 1260 AGGCTGCAAA GGAAATGAAG TTGGCATTCT GTAGTCCTCA CCTGGCATGA ATCACACACA 1320 GCCCCAAGGG ACCGGGACAA GGCTACATGT CAGACTGATG GACTATTGTC TGGAGCTTTG 1380 AGAGAGGAAA AAGGGAAGGC TGCTTGCAGG AGAAAGGTGA ACAGGTTGGC CCCGGCCCAA 1440 GAATGACAGA GGCGCCTTGC TCCTGCCACC CGGCTCTGCT CCTCTGGCCC AGGAACAATA 1500 ACAAGGCGCT GTCAGGAAGT GACACTAAAA TGCCTTTCCC CTTATACCTC GTTCAGCCTC 1560 TGGCAAAAGG AGGTTCCCGG AGGGAATATT TTTAGTTTGA CAAATGAAAG CCTGGGACCG 1620 AGGACAGGAG GGATAAAGGG AGCTCTTCTC TGACACTCCT GGAGACGGGG AGATGATGAG 1680 TCAGATACAG AGGGCTTAGG CACGACTTCT CAAGACATTC CTCAGGCATG AGCACAAGCC 1740 AGCCGCTCGA ATTCCTCCTG CAAGGCCCGC CACCCGGCAA TCAGGGCGGA GGGGCCGGGC 1800 CAGAGGAGCA GCTCTGCTCT GTCTTCCTCT TGGCACATTG TTGGACAGCA GCTTTGGAAG 1860 ATCAAAGCAG CCGCCTGTGT TGCTTTCCGG AACTGGGACT CAGGAGGCCT GGGTTCAAGT 1920 CCAGGCTTCA CCATTTGCCG GCTGTGACAT TAAGTGTCCT CATTTCTCCC TTTATGCCTC 1980 AGTTTCCTCA TCACCAAATT GAGAGTATTA TAACACCTTG GAATTATTAT TATGAGGTTG 2040 TACATTTGGA AAAAAAAACC TTGAGAATGC AGTGTTTAAA AGCATTGGTT TTCTGTATTG 2100 CTCCCAGTAC CCCATATGCA GATGGACTCA AAATCTCACA CTGGTGGCCA CGTGCAGTGG 2160 CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCAAAGGTGG GTGGATCACC TGAGGTCAGG 2220 AGTTCGAGAC CAGTGTGGCC AACATGGTGA AACCCTGTCT CCACCAAAAA TACAAAAATT 2280 AGCCAGGCAT GATAAATAGG TGCACGCCTG TAATCCCAGC TACTGGGGAG GCTGAGGCAC 2340 GAGAATAGCT TAAACCTGGG AGGCAGTGGT TGCAGTGAGC CGAGATTGCA CCACGGCACC 2400 CCAGGCTGGG CAACAGAGCG AGATTTGGTC AAAAAAAAAA TCTCACACTG GTAACAATAA 2460 TAACCAGTAC CTATTGAGTG CTTCTTACTT ACCAGGCTTG 2500
|