Tag | Content |
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EnhancerAtlas ID | HS060-29153 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:15621570-15622720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr6:15622538-15622548 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr6:15622538-15622548 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr6:15622538-15622548 | ATTTTCCATT | + | 6.02 |
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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 |
GH06I015621 | chr6 | 15621265 | 15623105 |
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Enhancer Sequence | ACAGAGCTAA TGAGGCCAGG AACTTAAATG AGGTTGATCT CTAGGCAGGC CAATTAATTT 60 CTCACAGACA GAAATTCTGT TCTAGGTACA AATTGTACTT GCTGCCCTAG TCACTCTTTT 120 GTTAATAACG TGGGGACCAG ATGAAAACAT GTGAGTGGTT TATCAACCTG GAATTCCTAA 180 TGAGAAACAA ACTGTACATA CTTCTGAATA GGACGGCCTC ATGCTCTTGT GCTGAATGAC 240 AAATTTAGAC TAAAAATGCT TGAAATAGTC CGTGGTCATT TTACTGCTAA CACCAAATTC 300 ATATTTATGT TCTCCCCTTT AAAAAGCTTC ACAGGCTCCC CAGCCCTTTC AAGTTAAACT 360 CCTTATCATT CAGAGAGCTA CTGCTCTCTG GCCACAAACT GTTTACTTCA CTTCTTTCCT 420 TCACATATTC TACATTACAG CAAAACAAGA GGAGTACTGA GCGTTGGTGC CTCCTCCTCC 480 TTGCCTCTGC CTGTCCCTAA CCCCGGCCTG TCTTTTCAGG CTTAGGCCAG TGGCAGCCCG 540 CCCTCCTCCC ACAGGGCTCC CTTCCTCTTC TGTGCTTCCC CAGACCTTTC AGCCTCACAC 600 AGGACTCACA TTCTGACTGA TATCATCCAA CCAGTTGTGT ACTCTCATAT CTCTCAGGAA 660 TCAGTAAGGG CCTTAAAGGT GCAGACTGTA TTTTTGCTTT TTTGCTATCC CCTAATAACC 720 CTGTCTGTTG AATTCAATAA AGAATAATTT CTGGTGATAG AATGATTTTA TTACTCTAAC 780 ATGTAAAATA ACTGAGAAGG CAAAACTATT CATGGTCATC TAGTTTAAAT ATTAAGAGAC 840 TATGCCAAAT TTTGTAAAAG AATAAACATG AGCAGAGAAC TTAGAAAACA TTAAACAACA 900 TGATGATACT TTTAGTATAT TAAACCAGGT CACATTATCA GTGACTTAAA ACAGAAGAAA 960 TGATGAAAAT TTTCCATTTT AACACTTAGC AGACTTGAAA TCAGTAACAA AATATAAAAT 1020 AATTGCATTG AAAAAAATAA AGGTTCATCC CCTTATATTA AACTTAAAAA AGCTCTTCAT 1080 ATAATAATGA CAAGTACATA CGTAATGTGT ATTCCGAATA TTTTATGTTG AATTTAAGTT 1140 AGCAGAAATT 1150
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