| Tag | Content |
|---|
EnhancerAtlas ID | HS112-07490 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr2:21278000-21279740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr2:21278801-21278812 | TAATTCAATCA | + | 6.14 | | Stat6 | MA0520.1 | chr2:21278983-21278998 | TATTTCCTGAGAAAG | + | 6.3 | | ZNF263 | MA0528.1 | chr2:21278751-21278772 | GAAGGAGGATGAGTGGGGAGA | + | 6.64 | | ZNF263 | MA0528.1 | chr2:21278754-21278775 | GGAGGATGAGTGGGGAGAGAG | + | 6.89 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATAAATACTG TTTTAAAATT TAAAATTTTA CTTTTTAAAT TGACAGAATA ATTATGCATA 60
TTCATGGAGT ACATTTACAT GGGATACATA TAATGTAATC AGATTAGGGT AATTAGCATA 120
TTCATCATCT CAAACATTGA TCATTTCCTT GTGTTGGGAA CAGTCAATAT TCTCCTTCTA 180
GCTATTTGAA GCTATGTAAC GTATTATTGT TACCTGTAGT CATCCTAAGG TGCTATAGAA 240
CACTTGAACT AAAATCTATC CTGCTGTAAT TTTGTATCCT TTAACAAATC TCTCCCTATC 300
CTTCCCGTTC CCCATCATTC CCAGCCTCTA GTATCCTCTG TTCTACTTTT AACTTCTATG 360
AGATTAAAGC TGGTTTCATT TGAGGCCTCT CTCCTTAGCT TATAGATGGC CATCTTCTCC 420
CTGCATCTAT ACGTGGTCTT CCCTCTGTGC ATGTCTGTGT CCTAAGCTCT CCTTATAAGG 480
ACAACAGTCA TATTAGATTA GGGCTCATCC TAACAACCTC CTCTAATCTC GTTACCTCTC 540
TGAAGATCCT ATCTGCAAAT ATAGTCACAT TCTGAGGCAT TTGGGGTTAG GGTTTCAACA 600
CATGCCTTAC TTTGCTCGGG CTGCCTTAAC AAAATAGCTT CAACAACAGA AATGTATTTT 660
CTCACAGTTC TGAAGGCTAG AAGGCTGAGA TCAGAAGGAG GGCTGTCTCC TTTGCTTTCA 720
GACAGCTGCC TTTTCACTGC ATCTTCACAT GGAAGGAGGA TGAGTGGGGA GAGAGCTCTC 780
TGGCATCTTT TATAAGGGCA TTAATTCAAT CATGAGGGTC CTACCTTCAT AAACTCATCT 840
AAACCTAATC ACCTCCCACA GGCCCCATCT CTTCATACCA TCACACGGGG GATTAGGGCT 900
TCAATATATG GATTTTGGGG GGCAGAACTG AGCCCCTAAT AGCTGAACGG GAACCGCAAA 960
CAAAAATAGG TCTACACTTC TGGTATTTCC TGAGAAAGGC TTTTAAAATC TTTGATAAGA 1020
TTCTGTCAAC TGACTAGCTG ACCAGGCACA GTAGTCCTAA TGGTCTTGAG AGTGCCTCGA 1080
ATGTGGCCTG CCCAGTGTCT GAGTGCTTCC TGAGATGGGC TTTGGTCATG GTGTGTGCGG 1140
CAGTGGAGAA AGGTTGGAGG TTGCCTCTAG GGCACAACAC TGGCAGATTT GGTACTGTAC 1200
TCTGGTGACC ACACAACCAT GAAATCCTGT GGCATTCATT CCAGGAGTAG GACAAATCCA 1260
GAAAACTACT GCCCTAGGAC ACTCATAAAG CCTTTCAGCA GCAGCAGAAT AACCCAGGAA 1320
GAAGAACGAT AAAGCTTGTT GACTTTTGCT CTTTGGAGGC TATCTTTCTC CTAGCAGAGT 1380
AAACGCATCT CTAGGGGATT AAAGGCAGGC TCCAGAGAGC TATCGACTCC CACGCACCTT 1440
CAAGCCAGCA ATCCTTTTAG CTCAAGAGAT AACATAGCCG CTAACCTTGG CCTTCTCAGG 1500
AAGGGCAGGT CAGGGCTTTG ATGCTGTGAG TGATTTTGTT GGGAAACAAG AGATATAAGG 1560
GTGTCCCTTG CAAGAAAGAA ACACACTATA AAAAAAACTA TAAATTAGAA AAAGATTTAT 1620
TTACATGAGA TATTAGGCTT CTTCAGGAAA GTACTGGAAG AAATATTTTT GGCTATTCAT 1680
TTATGAGATT TTTAAAGTGA CATCATTGAC ATCAACCAGC CTAAAAAGAA AGACACAATA 1740
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