Tag | Content |
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EnhancerAtlas ID | HS187-10100 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:16132850-16134230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr17:16132962-16132972 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr17:16132962-16132972 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr17:16132962-16132972 | 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 |
GH17I016229 | chr17 | 16132921 | 16133130 |
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Enhancer Sequence | TTAAATTTTT TGAGAATTGA CAAACTGTTT TCTGCAGCAA CTGTACAGTT TTACGTTGCC 60 ACCAGCAATG AACTATGGTT CCAGTTTCTC CACATCTTTG TCAGCATTTG TAATTTTCCA 120 TTTTTTGGAC TATAGCCATC CTAGTAAGTG TGCAGTGATG ATGTCACATT GTGGTTTTGA 180 TTTTCATTTC CCTGATGACT AAGGATGATG AGCATCTTGC ATCTTTTCAC ATGCTTATTG 240 GCCATCTATA TATCTTCTTT AGAGAATACC TATTCAAGTC CTTTGCCCAT TTTCTGATTC 300 TAGTTTCATT TTAAAGTCAT GATTTTTTTT TTTTTTTTTT TTTTGAGACG GAGTCTCGCT 360 CTGTCACCAG GCTGGAGTGC AGTGGCACGA TCTCAGCTCA CTGCAACCTC CACCTCCTAG 420 GTTCAAGAGA TTCTCCTGCC TTAACCTCCC GAGTAGCTGG GACTACAGGC GTGTGCCCAC 480 CATGCCCAGC TAATTATTGT ATTTTTAGTA GAGATGGGGT TTCACTATGT TGGCCAGGAT 540 GGTCTCAATC TCTTGACCTC GTGATCCACC TGCCTCGGCC TCTCAAAGTG CTGGGATTAC 600 AGGCATGAGG CACTGTGCCT GGCCAAGTCA TGATTTCTTA GACTGGGTTC TGTGGACACA 660 TCCTAATAGA AGAGGATCTA GCTCTCTTAG TTTCAGCTTC CTTTGGGAAC CCAGGCCTCT 720 GGGCTCCAGT AACACTGCCT CCTTCCTTTA CCTTGCCAAC CGAGGGTTGG TAGTCACTTC 780 TTGCTATCTC TAAACTCTGG GTTACTTCAC TGTTCCTTTT GTCCCTTAGA TCCTCCCTCA 840 GTTATGCGTC AAAATCTTTG CATTAAATTC TTGCTGTTGT AACTATTTGA TGTGGTTTCT 900 GTTACCCCGA ATAGATCTTG ACATAGCATC TAAATTCCCT CATTTTATAG GGGAAGAAAC 960 TTGTACCATT TTGTCTTCCA AATACATTTT AGAATTACTT GGTCATGTTA AAGGAAAAAC 1020 ATTGCAGCTA TTCCTTCCCA TAACATACTT CTCAGTCGTA ACTAGCAATC TAGCAGTCAT 1080 AATCACTTTT TTTTTTTTTT GAGATGGAGT CTCACTCTGT TACCAGGCTG GAGTGCAGTG 1140 GCACAGTCTC AGCTCACTGC AACTTCTACT TCCTGGGTTC AAGCTTTTCT CCTGCCTCAG 1200 CCTCCCAAGT AATTACAGGC TAGGATTACA GGCCTGAGCC ACCGTGGCCA GCCTCATAAT 1260 CACATTTAAT ACAAAATAAA GTCACGTTGT AAAGACTCAA ATTTATACAT CACAATGTAT 1320 AAAGGTAAAA ATTTTATTTT TAAAGAATAA AATTACAAAA ATTAAAGAAT TTCTCCAAAT 1380
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