| Tag | Content |
|---|
EnhancerAtlas ID | HS095-14664 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:13023120-13025300 |
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 | chr19:13023797-13023807 | ACCAATTAAC | + | 6.02 | | ZNF263 | MA0528.1 | chr19:13023139-13023160 | CTTTCCCTTCCTGCCTCCTTC | - | 6.53 | | ZNF263 | MA0528.1 | chr19:13024785-13024806 | CCCTCCTCTCACTCCTTCTCC | - | 7.48 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 13023589 | 13024232 | | chr19 | 13024661 | 13024953 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I012911 | chr19 | 13022750 | 13026005 |
|
Enhancer Sequence | CAGCCTTTGC CTGGAATGAC TTTCCCTTCC TGCCTCCTTC ATAATGGAAC ATTTGGAACT 60
TTTGCTTCTC TACCCCCCGC TATACCTAGG CCTTGCTGGT CACAAAGCTG CCAAAGTTTA 120
TGAACATCAG TCCCCTCCAG CGCACGACAC CTTGAGGGTG CAGACTACAC CCTACTCATT 180
TGTTTTGCAG CACCCCAAAG GTTTCATCAG TTTGCTGAAT ATCTAAATGA ATGCAGCACT 240
GACATTGGGG CTCCCACACC TCCTCGTACC CAGTTCACCT TGTTGTCTCA GCCTCTCCTG 300
GATGCTCTCA ACAGTTTCAG ACCCTAAAAT TAAAATCGAT GAGAGCACCA GGTGTTTCTT 360
TTTGTGTGAT TGTTCACAAC CTGCTTGAGC TGCTAATGGT TCAGAGCTGC TCCTTTTTAA 420
GGCTCAAGGG ATGAGGCTGG AACCGGTTTT CATGGCAGCT AAGCAAACAG TAAAAAAAAA 480
AAAAAATCAC TTGAATTCAG CTAATTCGAG TTTCATGGTA GGACAAAGGC CTGCATCAGA 540
TGTCTGCTGA GAGCTTCTTT ATTTTTCCAA CCTCTCCTTT GGGGATTTAT CCCTTTTGAT 600
TTCATTTTTC TTAATACACA GCAGCTGCAT ATTAATCAGG ATGCTAATGA ATCATAGGCT 660
TCCCTGGGCC TGCATTCACC AATTAACTTT AACAAACAAA ATGCGTGGTG TCCTCTCTGC 720
TGGCTTTCCC GGTTCCTAGG CTGGCTTCTG TTGCCGAACC CTGGACCGAG GCCAGAGAAT 780
GCAAGTCAGC CCAACACAGC ACGTCGGGTG TGCATGGCCT GCGCCCGGAT TGGGCAGCGG 840
GCTGGGGGCT GTGAACACAG CGCTGCGTTC ATCTATTATG GTCTGTCCTT CTAAGAAGTC 900
CCTAATTTGG CTGCGAGGAT TAGGACATAG TTCCCAAGCA GGGCCCACGC TGGCAGGGGG 960
CCCAGGAGCT GCGGAGGAAA TGGGTCTAAG CGAAGAGACC ATCTGTTCGC TCCAGGTAAA 1020
GCTGTGATTG GCAGGCGACT GAGCCAGAAC TGCCCGCTGG TGGGGCCCTC CCTCCGTGGC 1080
CTCTAACAGA TATACAAGTA AACAATCCGC CAGCCACTTA TGACCACCGA GGGTGGCAGT 1140
CCCGGGAGAG GAGGCAAGCT AATCAAACAT TCAAGGGGGG AACACAACAG AATCTCTGGC 1200
GCTTGGGCAA AACAATGTTT TGCTGAAGTA CAGCCAGGAA GGGGGAAGGT TTGAATGGAA 1260
GCTGATGAGC CAGTTCCTCA ACCTCTCCTT TTCTCTCTGG AAACGTGTTA ACATTTTAAT 1320
CATGTTGCTG AGTATCTGCT GCTGGATCTA TTAACTGGCC CCTGCACTGG TTTTAATCTA 1380
TCTGTTTTTT GGCCCAGGGT TCCTGTGGAG CTCCTTGAAG TCTCTAAATG ATTTGCAGCG 1440
GTCTGTGTCT CTTCACTACA CAGATCCTGG TCTAAACATG CTATTCCGCA GTAAGGTATT 1500
AGCAAACAAA CGACTTCAAC CATTGCTTCC CTTTTTTTTT GGTCTCCAAT TGACAGCACA 1560
CACCTATAAA CCATTTCACG CGTGGCCTGC TTTCCAGCAG AGGAATGTGC GAGGAGAGGG 1620
AAGCTGGCTT GCTTTCTGCC TAGAGTCCTC AGGGCCCTGT CCTGACCCTC CTCTCACTCC 1680
TTCTCCAGGT GAGCTCATTC ATTCCACAGC TGCTGCTGAA ACAATGACTC CCACAGAACC 1740
ATCTCCAGAC CCTCACCCCA CCCCGAGTTC CGGGTCAGAA AGTTGAACTG TATCCTGGAC 1800
ATGTGGATGT CCCTGGCCAC CGAAAGTGGC TCAGATAAAC AAGGACAACA CAGAACTCAT 1860
GTTCTTGTCT CTGCCAGAGA AGCCACCACC TACCGGAAAC CACCACAAGC TGGAAAGCAG 1920
ACAGCAGTGA TGTGCTTGTA AGCATTTAGC AACTGGCTGT GTGATGGGGG GGAAGCCCTG 1980
ATTCGTAGTG TTTGCCAATT TCCGTGGTGC AGAGCCTCCC ACCATTAGCC AATTTCAGGC 2040
TACCAACATG AAGACGCTAA ATGCCAAGTT GGGAAGAGAT GTGTAGAATT GGCTCTTTCA 2100
AGCCGGTAGG AGCTGGCCCC AGTACATCAT GGCCGGGAAA CATCCTCCCT CATCCCCTTC 2160
CTGTGTCTTA TGGCACAAGG 2180
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