| Tag | Content |
|---|
EnhancerAtlas ID | HS176-11862 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:98904480-98906630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr13:98904839-98904850 | TGCTGAGATTT | - | 6.32 | | MEF2C | MA0497.1 | chr13:98905138-98905153 | TGTTATTTTTAGAAA | - | 6.17 | | ZBTB18 | MA0698.1 | chr13:98905972-98905985 | CAGCCAGATGTGC | + | 6 |
|
| | 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 |
| GH13I098252 | chr13 | 98904403 | 98908905 |
|
Enhancer Sequence | TCAGATGAAT TTTTCAAAAT GCCCATTTGC ATTTTGACTG TTCAGACTTC CTGACTATTC 60
AATGTGAGAC TCATAAGACT AAAAGAATAT CAGTGCATGT GATGTGACTC AATAACTTTA 120
AGACTTCAGC GTGGCTCTTG TCAGGTTCAC ATTCATGTTC TTGGGTAGGT TCAATAGAAC 180
GTTCATTACC TGCATATTTT CATTTATTAA AATTAAAACC GACCCCAACA CAGAGTGAAG 240
ATGACTTTTT CACATTACTT TGACTTGTAC CTCAAAGACA AGCCAACAAT GGCCCAGCTA 300
ATGGACAGGA GTGCCCTGGT GGCAGATGGT CTGGCTTGAC CCTCATGGAT GCTACCAAAT 360
GCTGAGATTT CCTCTCACAG GCTGCTGTAG AATGTGCCCT CCAAAATGCC AGGTATCTCT 420
GTACTGTGTT CTTTAAACAT TTATTGAAGA CCTTTGTCTT TAATACCCAC CCACTTAGTT 480
GCCTGTGCCT TCCCAGGACC TGAAATTGGA TGTAAGTCAA TGTCAAAGAA AGTGTCCAGT 540
GTTGTTCTTT AAGGAAGATT ATCTATTATC CTGCTCTAAC ATTCAAGTCA GCGACCCAGT 600
GAGCCCCGGT GATCATGTAT ACTTCAGAGG AAAATATATC TGCCTCAGAT TCTCAGGGTG 660
TTATTTTTAG AAAAATACTT CCAAATTGTT TGACACCAAC ATTTTTCAAC TTGATTTTGG 720
CAAGCATAGG CCCCTGAGAT TTTAAAGTAG CTTTTATCAA AACAAAACTA GCTACTTAGC 780
TATGACTGCG TAGAATTCCA AAGGTTGGAG AGAACCTTGG TGGCACCCAT ACTCAAAGTA 840
GGGAGTGTGG TGCATTAATA GCTGTATGTT GATTTAGTCT GCGACGAAAG CAATGTTCAA 900
GCCAAGTTTG TCCAGCAAGG AAAAATGTTA AGTTTCTGAT CTTTAAAAAG GGTGTTGAGG 960
GAGATGAAAA TTAATCTGAA GCATTAAGGA ATGCTGTTAA ATGCTTGTTG GCAAGTAGTC 1020
CTGAGTTTAG CCTTTTATTT CTCTTAACCC ACTGCTGGGG CTGCAGAAGA TGACGCCAGT 1080
GATTGGTAAT AAAAGTCTCA GTAGCTGCCG TTGACTGAGT GCTGTTGCAG AGGATTTTCC 1140
TGATGCTCTC GCAGGAAATG CCCATAGCAA CCGCATGAGT CAGATATCCC AATCTGGCTT 1200
ATCAGTGAAG AAACTGAGAC TCAGATCAAA GACTTTGATG TGAGACAAAA ACTGGATTTG 1260
GACCCTGCCT GCCTCTGCCA CTTTTAAACT ATGGCCTGGG TTTCACCATT TGTGAAATGA 1320
GGATGATGGT CTCCACCTCA AAAGGTGGTT GTGAGGATTA AGCGAGATGA TGTATTTATA 1380
ACAACACATC ACTTACAAAG TAGGAAGTGT AGACTGCTGT GGGCTTTGCT GCGTTCATCC 1440
AAGGTCGCAC CGCTAAGTCA TCGTTGAGCT CGGTTTCCAG CCCAGATGTT TCCAGCCAGA 1500
TGTGCTCTGC TCTTGGCCTT TTATTTTATA GTTGCTGCAT CAGTTCATAG CAAACATTTC 1560
ATGGAAACTG GGCCATGTGG TTAGTTTTAG GTTTGCTGTA ATGAAGAGCG CCCTGGGTGG 1620
AGGCAGAATT TCTGGGTTTG AGGTCAGAAT CCACTGTCTT GTTTGTGTGT GTATGACAGT 1680
TTTCATGCAT GCTTTCCATG TGGGGTTTGG AACAAACTGA TGGGCAGTTT TGGCTCTTCA 1740
TAACACAAAG TGGGGCTCAT CGCATAGTTA TATACAGCTT TGAAAATACC ACTCTGTACT 1800
TCTGATGCAT GTGATCATTT CAGGGTTCTG AGACCACCCC AACTCATTTG CCCATCATTA 1860
TGGGACCTCT GAGTTTCCGG GCAAAGTGAT AATCTGAGCG GGCAGTCGGT AGTGTGTGGG 1920
TGTCCCTGAA AAGTACTAAG TGTTCTCCTC ACTTGTTCCC AAATACTCAT CTCATAATGA 1980
TGCACTAATA CATGCCATTA TTGGTGTTTG TGTCATTTTT GGATTTTGAG GTTGAAGTTG 2040
AAGAGAGATG ACAGTTTAAT TCTTAGCTCC GCTCTTAAAA ACTATGGGAT TCTGAACAAA 2100
TTTCTTAACT TTAGTGAGTG CCAGTTATAT CATCTGTAAA GTGTGGATGA 2150
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