Tag | Content |
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EnhancerAtlas ID | HS187-10216 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:26136720-26138580 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr17:26136759-26136770 | TTTTATGGCTT | - | 6.62 | IRF1 | MA0050.2 | chr17:26137450-26137471 | CATCAGTTTCAGTTTCTTCTT | + | 7.25 | IRF8 | MA0652.1 | chr17:26137454-26137468 | AGTTTCAGTTTCTT | - | 6.03 | KLF4 | MA0039.3 | chr17:26137515-26137526 | AGAGGGTGTGG | - | 6.02 | ZNF263 | MA0528.1 | chr17:26137648-26137669 | AAAGGAGGGGGGACGGGGAAA | + | 6.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 26137153 | 26138055 | chr17 | 26138067 | 26138207 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I027809 | chr17 | 26136851 | 26139775 |
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Enhancer Sequence | TGGGGTTCAT TCACGTGGCA TGTTTAAGTT CTTCATTCTT TTTATGGCTT AGTAATATTC 60 CACTGTATGG ATATACCACA TTTTATGCAT CCATTCATCA ATTGATGGCC ATTTGGGTTG 120 TTTCTATTTT TTGGTCACTG TGAATATTGC TGTCCAAATA TAAATGTTTG AGTACAGGTT 180 TTTGTGTGAA CATGTACTTT CAATTATCTT GGAATAGAAT TGTTGGGTCA TAGGGAAACT 240 TTATGTTCAA CTTTTTTGGG GTACTGCCAG ACTATTTTCT GAAGTGGCTG CTGCACCATT 300 TTATATCACT ACCAGCATAG GAAGAGGGTC CCAATCAGTC CACATCCTTG ACAACACCAG 360 TAATGGGCTT TCTTTTTTGT GTCATATAGC TTCTAGTGGA TGTGAAGTAG CCAATGGACC 420 ATTGACGAAT GAGTGAGTGA CAAACGGATG GATGGATGGA TGGATGGATG GATGGATGGA 480 TGGACATATG GGAGTAGATA CCTGACCCTG AGTTCTGAGC TCTGATTTTG GTGGGACAGC 540 CTGCTTCCCT GAGGACCTGC ATCAAGTAGA GACATAGCAA CCTGCAGCCT GCCCCTGACC 600 ATCGTGGTTC CAGATGTCCA ATCTGCCTTC GTCCTCGGTG GCTCTTAAGC ACACAGGTGA 660 CCTGGATTCC CCTAAGCCTG TGGAAGGCCC TGGAGGGGGC CCCATTCTGG GTGACACAAG 720 TTTTATTACT CATCAGTTTC AGTTTCTTCT TCTGTGAAAT GGAAGGAGAA AGAGAAAAGT 780 CACACAAGTT TCTGCAGAGG GTGTGGCACA TAGCAGGTCC ACAATAAATA GGAGTTTCGT 840 TTTTCCAGTC TGTTTCTCAT CCAGTGTGTA TATAAATGCC ACTCCACTAA TTATCTACTG 900 GAAAAGAGCT TGAGAAGTGG GGCAGTGGAA AGGAGGGGGG ACGGGGAAAG CCAGGCAAGA 960 GATTTACATA TGGCAGGAAG CTGCAGCAGG TCATCGAGGG AGTGGGAGTC ACAGAGCAAC 1020 CCTGGGAGGA TTGTCACAGG CTTCGGAAGA GGATATCCTC CCAGCCATTT GCATACCCAA 1080 GCACCACTCT TACTGTCAGG AAGACCTGAG CCTCCTATTT AGGCCTTTGG ATGGGTGTGG 1140 AGAGAGGGCA GCATCTAACT AGTGCTGATC TGAGATCAAC TGCAGGTCCC CAGGCAAACC 1200 CCACAGAAGG GTGAATCAGA TTCCAAGGCC AGTGAATTTT ATCCATTGTG CCAACCTTCA 1260 TAGACAAGGA ATGGCTGCTC AGAGCCTTGC AGTGAGATCA ATGTTAAAGT TCTGTAGTTT 1320 TAAGGCTCAG TAGGAAAAAG TAGCCACCCG CATCTGCCCT GGGCAGATGA CCAATGACCT 1380 GTATTTACTG CCCCTGTTCT AGACCAGTAC AAGATTAGCT GTCTGTTGGG TAGTTTCCAT 1440 GTAAATAGTT TGTTACCTGG GGCAGTTGAA AGGTCAGGAG GAAAAGAAGA GGGGATTAAA 1500 ATAAATTGCT GGAACGGGGG ACTGGCGGCG GCAGTGGTGC TCACTTGAGG CTCCAGCCTG 1560 CAGTGAGCAT TGAGCACTTA ATTTATGGAG TGCTCAGCTG AGGTTGCCAC TAGCTGCTTA 1620 CGAGAGGCCA GCAGCGCCGT GAGCCAGGCC CACTTAGGGA AGATTCTTGG CTCATCCATG 1680 TGACTCACCT TCCTCATACG TAACATGGGG ACAATGGGGA TATATGTCAC AGGGCTGCTG 1740 TTTATCTTGC CGGATGATCT AATGCACATG GATGAAGAAG GGAATGTGGG AAATACATGC 1800 TCTCAGTCTT AACAGAAGGG AAAACTGAAG CCCGCAGTGG GTTGGAAGAG GTGGAGAAAA 1860
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