Tag | Content |
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EnhancerAtlas ID | HS187-13995 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:137180500-137182230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:137181190-137181209 | TGTCCACAAGGTGGCAGGC | + | 6 | NR2F1 | MA0017.2 | chr2:137181582-137181595 | AAAAGGTCAAAGG | + | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 137181216 | 137181600 | chr2 | 137180800 | 137181124 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I136423 | chr2 | 137180771 | 137181582 |
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Enhancer Sequence | CGATGCGGCA CCTAGATTCT GAGTAAATAG ATTGGAGTGA GTGGGGCATT GACATTTTCA 60 AAACCTCCCT GGGAGATCCT GACACTGCTT AAAGTTTAAG AAACTCTTGG CCGGGCGCGG 120 TGGCTCACGC CTGTGATCCC AGCACTTTGG GAGGCCGAGG TGGGCGGATC ACTTGAGGTC 180 AGGAGACCGA CCACTTTAGG TCAGAGTTCA GCCTGGCCAA CATGGTGAAA CCCCGTCTCT 240 ATTAAAAATA CAAAAAGTAG CCGGGCGTGG TGGCTTGTGC CTGTAATCCC AGCTAGTCGG 300 GAGGCTGAGG CAGGAAAATT GCTTGAACCC AGGAAATGGA GGTTGAAATG AGCCAAGATC 360 GCGCCATTGC ACTCCAGCCT AGGCGACAAG AGCGAAAACT CCCTCTCAAA GAAAAAGGAA 420 AAAAACTCTT AGTTAACACT AGCGTTAACC CCAAAGTTAA AGGTGAGTCT GGTTTGGATT 480 TGGGGCATTT AAAACTTGCA TCACCCCTGA CATAAAAAGT CTGAATTATG CGGAGAAAAA 540 ATGCTCCCCA AATCCTCCTC ACGAGCTAAT TTTGCCGAAC GAATCCGCTT CTCACCTGCA 600 TTCGCGCCTC TCGCCGCCTT TCTTTCAGGC GCACAGAGAT AAGGTGGGCA GAGGGCACTG 660 GAGCCAGCCC ACCGGCGGTT TTACTCCTGG TGTCCACAAG GTGGCAGGCC AGGCACTTGG 720 ATTTGCGCAG CCAAGGGCGT GCGCAGCCCG CGGCCGGAAG CGTCCCGGCA GATCGCAGAC 780 GGGGTGTTGA GGGACCCCGC GCTTTTGCTT TCTTATGATT TGGGGGCTGG TACCTGGGCT 840 AGAGCTGAAG CCGGCAGGTC AGTTTCCTGG GAGCAGGGGT GTGTCTGTTC TCAGAGAAGG 900 GTTTAAGCCG ACTCCCACGT ACGCCCTGGA GGCCATAAGA GCATCTCAGA GGCACGCAGG 960 ACCTCCAGCG TGTGCACGAG TGTTCAGGGA TAATGTGAAC AAGCTGTTCT GTTTTTTTTG 1020 TTGTTGTTGT TTGTTTGTTG TTGTTTTTGG AGGGCAATGT TTTGGTGATA GTTTTAAATA 1080 CTAAAAGGTC AAAGGCAGAA TAGATGTTTT GTGTGGTTTG AAAACTCCTC AGTGGAGGGC 1140 CGAGGACTCC AGTTAACATG CACTTGCTGT TGGATATTTT ATGGGCATTT AAAATATATG 1200 GACTTGCTCA CCCACTTCAG GCTTTGACCC AGCAAGGGGA TGCAGTCCAT AACAGTAAAT 1260 GAGTCAGCGA GTGGCCTGGT GACACGTTAG GATGAAAAGT GGAGGGGGAA TTTTTATATG 1320 CTTTTAATAT GCTGTTTGTT CCTACCTCAA GCTAGGACAG TGGTTTCCTG TAGGTACAAA 1380 ATGCTTGCAC GTGGTTTAGG GCTCCTGAAG ACACGAGGAG GCAGCCCAAA GAGCAGAGGC 1440 TTGGGGTTAG ACGGGCACGG GCTGCACCTC CAGCTCAGCC TCCCACCAGC TGTGGGATTT 1500 GAGACTGGTA CCTCATCCTG GCTGAACCTG AGTTCACTCC TCTGTGCGAT GGGGATGAGA 1560 ATCCTGGGGT GGGGTGAGGA GTAAAGGAAA TGCAGTTCGT CTGTTCCCTC TTTTAGCACA 1620 CACAACTTCA CCACCTGTGT GCCAGGCACA AGAAGGTTCT GAGGATGCTA AGGCAATCAG 1680 GCATGGTGAT GCCTCCCAGG CAGATATGCT GAGGGGTGTT TTCAGTTCAG 1730
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