Tag | Content |
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EnhancerAtlas ID | HS187-14884 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:239402290-239403770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr2:239402701-239402712 | TATGTAAATAT | + | 6.62 | Zfx | MA0146.2 | chr2:239403283-239403297 | CAGGCCGCGGCCGC | - | 7.58 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 239402800 | 239403200 | chr2 | 239402549 | 239402790 | chr2 | 239402574 | 239402800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I238494 | chr2 | 239402842 | 239403041 |
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Enhancer Sequence | GGGGTCTTGC TGTGTTGCCC AGGGGGTCTC GAACTCCTGG GCTCAGGCGA TCCTCCTGCC 60 TCACCCTCCC AAAGTACTGG GATTCCAGGC ATGAGCCACC GCACCCTACC CAGGGTGTTA 120 TCATGTTTGG TTTATATATA ACGTCCAGGG CTTTTAGTTG TACTTAGCAG AGGAAAACGG 180 AAAGTAGGTC TGCTTCACCT TCCTGGAAGC TAATATCCAC ATACATTTCC TTGATAATCA 240 GAAAAATTAA AATGCAATCG TGTTTCACCA AGTGCTACAG AGTAGTTAGG TTGAAGAAAT 300 TAGAGAATAA GCAGAAGGCT GCCTTAAAGC TGAAATGCAT CTGAGCAAGG ACTCAACGGG 360 CCAGTGGCAA CAGTTCTGAA CCACAGCACA GCTCTTTTGC TTATAAACCT CTATGTAAAT 420 ATTTTGGCCG GAATTTCCCA TGCAGCTTTG TATGTTTCCA TTCATTCAGC CCTAGGAGGG 480 CTGATGCGAG GAAAGGAACA GAACAATCGC AACCCTGTGT ATTTCACACA ATTAATACCC 540 GAGAAATGGA ACCTGCGTGT CCCCCTTCGT ATTTGGCTCT GGCTTTGAGC TGGTCCAGTG 600 ACTGTTTTTC GTACCAGAAG TCCCTCCCAG AAGGTCTGCT TAAGTGTTCA AGCAGATAGG 660 GAAAGCGCAG GAGGTGAGCG TGCAGGTGGG CGAGGTGCAG GCTCTGCTCT CCCGGCAGCC 720 CGTGCAGGCC ACAGGCTTCC TGTCTCTGCT CATCTAACCT GAACCATCCT AGGAAGGGAG 780 GCAGCGATGA GGTTTCCTGA CTCAGAAGGA AGCTGAAAAC GACCTTAGCC CTTTTTATTG 840 CACTTCCTTT TCTGGGCCGC ACAGGAGGGA GGCTGGGTCA GTGTATTCTG AAGATGAAAT 900 GTGGAGGTGG CAAGACCTGC GGAGTCCCCG AACCCTTGGC CCTCTCTCCG CACGCCTGCG 960 TTTCTGCTCC TGTGTGCTTG TCTGTCTGTG ACACAGGCCG CGGCCGCATG GCTGAAGAGA 1020 GGGGATCCCT ATTTGCTCTC CTGTCATTAT TGCTGTCACA AAGACCATCC ATGCCATTTG 1080 CCTCTGGGGA ACAATGATGT CGTTTGGGTT CCTGGATGCC CTCACGCCAT TCATTCACGC 1140 ATCAAACATG TGCGAGGTGC TGACTCGCAG ACAAACTCCG CGTGCTCAGC ATGCTGCTCT 1200 CACAAGATTC TCGGCTCTTC TCTGTCCCTC TAGTGACATT CTCATGGGAA AACATACAAT 1260 TGCCCACCTC ATATTCACAG AGAGGGTCTT TTCCATTGCC TGGCGGTCAA AGGGAGGCAG 1320 AGACTGTGAT GACACAGAAA GGCCAGGCAA GCCCTTCCCC ACACTGGGCC ACTCCAGGGA 1380 ACACTGGTTT TGATTCATGC ATGGCAGAGT CTCCACACCC CAGGTCATTG TCCTACCACC 1440 TTTTTCAAAA CTGGGGGAAA AATATGTGCC TGGATATTAC 1480
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