Tag | Content |
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EnhancerAtlas ID | HS037-41441 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chrX:13149300-13150460 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chrX:13150118-13150129 | AAACCACAGAC | - | 6.62 |
| | 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 |
GH0XI013131 | chrX | 13149720 | 13150250 |
| Enhancer Sequence | TGATTGCAAA GATAGATACA GAACTCTTGT GTCCTACACG GCAATAAAAC TGTAACCTTT 60 GGATTTTGGG GGGGTTTTTG TTTGTTTTGT TTTGTTTGTT TTTTTTTTTG GTTTTATTTT 120 GTTTTGTTTT TTACCGAATA GAAAGGAGCT GCAACTCTAC TTTGCAAAAG TCATTTGTAA 180 CTTATCAAAT TACCAGTTAC AATCTACCTT CATAGAGTAG ATGCTTCAGA TCCTAGTCAG 240 TCATAAATAG GTAAGTCAAA CCATGGTGCA TTTCCCTAGA GAATGAAATA TTCCTGGATG 300 GTTTTGGTAG ACAGTGCTTC AGTATGAGTT GGCAAGGACA TGCAGTCATC CTTTTGCTTA 360 TTTCCAAGTG TTGTATCACT TTTCTTCACA GAGCCACACA AAGGCATTCT GTCTACAGTT 420 TAGTAGATGA AGTTTTGTGG GTCTTGGTGG CTGAAATACC CTTGTAACTT CCCTCAAAGC 480 CCCACGTCAT AAAAAGCTTC AGCAACCAAA GGAAAATGCT AATGTTTCAA AATGGAACTC 540 TTGAAAGATT TGTCTTTCTA AAAACAAGCT TTTGTCATGC ACCCAAGGCA AAGGTGGCCC 600 CCATCTCCGC CCAGCACCTC ACTTGACTAT AGGGCAGCAA TCTGCAGTGG ACTGTTTGTC 660 AATGCTCCAT TGTATGCTGA GGTTCTGAGG GGTGTGACCA CCCACAGCTG GCCACAGCTC 720 CTCCATTTAC ATTTGCTAGC CCACGCTTGC AGCCAGAAAG CCTTTTAGAA TGTTGCAACA 780 AACAAAACCA AAAGCCCACA GGCCATCTCA GGCAGAGGAA ACCACAGACA GACACACTGT 840 CTTCCACAGG CTCCCAACTC TAGTTGACCC TGTTTATGTC TTAGTATTTT AAGTCTGTGA 900 CCTTAGCAAA GGTTCAACAT GCAGTGCCAA CTGAGCAGGC AGAAACAGAA GTACAGTTCT 960 TGCCACAGGA TTTGGAGGCA CAAGAATTCA ATTTGAATTC TGTGTCCACC ATGTACACAT 1020 CATGTAACTG TACCTGCCCT GAGTCTTGGT TTTTTCTTTT TTTTTTTTTT CTCTAATTGT 1080 TTTGGTATCT ATCTATCTTA AGGTAAACAT GGTTTTGAAG TAATGTCACT TTTTTATTTA 1140 TTTTTTATTA TTATACTTTA 1160
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