Tag | Content |
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EnhancerAtlas ID | HS187-14130 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:161522680-161523620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr2:161522961-161522975 | GTGACTCATTTCCT | - | 6.22 | MNX1 | MA0707.1 | chr2:161522815-161522825 | TTTAATTACC | - | 6.02 | RFX5 | MA0510.2 | chr2:161522996-161523012 | TGTTACTCTGGCAACG | + | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I160665 | chr2 | 161521898 | 161524306 |
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Enhancer Sequence | TCTTCTGAAT TATCTCAATG GGTATTGCTC CCCCTCCCCA GGCCCTCTTA GAGGACTGAT 60 TGTGGTTTGA GTGCTCTCAC CCTTGCATTT GCTATGTGCT CCTGTTTGCT TGAGTGTTTC 120 TTTTATCCAG TTCTGTTTAA TTACCATGCA AAACCCTCTG TTGAGCTTTT AATTAGCAAG 180 TTATCTCCGT CTGAAGACTG GAAACCCTGG GCTCTTTCAG CATATATTAG ACAGCTAAAA 240 TATGAAATTA AAGAAAACAG AGTTTTAGCC AACAGAAACA AGTGACTCAT TTCCTTGTGA 300 AAACACACAA GGTTTATGTT ACTCTGGCAA CGATATTCCA GAATAGCATC TCTCCCCTCC 360 CCTGTCAGAG CTTTTATGTG TTTCTGTTAC AGTCTGTGTT CCACAGTGAC CTAATGTTGA 420 ACCAAGTCAC TTAGTGATTC ATCAGACACA AGAGAACTGT GCTTTCATTT AGATAGCTCG 480 TCCTATGTCC TTTTGACCAA AGGAAGAAAA GTTTACTTTG TATGAAGAGA GGAACTGTAA 540 AAGAGATATA AAGAACTCTT GACTGAGTGC TGTCTTAGGA TGTAAGTGTG GTCCTGCTGT 600 TACTTTAAAA ACACCACAAC TGGTTCCAGT GTGTTAGAAT TCTAAGAGCC TATTTTTCTA 660 GACAGCTGAT TAAATCATAA TGTGCAACCT GTATATGTAC CACGTAGGGA AATGAAAATT 720 CAGAGACCCA TTGCAGAAGA CTCCAGATGT TTCTTGGGAC TCACATCGTG GGAGGGAATA 780 TCACAGTGCT TAGGGTCAAA ATTTTAACCC AAACCACTAC AACTCTCCAA AGCAAAAATG 840 TGTAGAGCAA AAACAGTTGA ACTAACTCTC TCTTCTAGGT TTTAAATTCT CTGAGGTACT 900 TAAAAGGAAG TGAGGAGAAC CTTCAATTTA TTAAGCTCTT 940
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