Tag | Content |
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EnhancerAtlas ID | HS007-15017 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr6:158662900-158664290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:158662990-158663011 | GGTTAATTTCACTTTCTTCTT | + | 6.34 | Zfx | MA0146.2 | chr6:158664062-158664076 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 158663221 | 158663364 | chr6 | 158663429 | 158663957 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I158241 | chr6 | 158662918 | 158664315 |
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Enhancer Sequence | AGGCATGAGC CACCGCGCCA GGCCAGCTTT GTTAAATTCT ATAGCTTGTA GTTGTTTCTT 60 GGAAAGCTTA AACTCTACTC TTTCCGCATT GGTTAATTTC ACTTTCTTCT TGGAGTCAAA 120 GACATTTTGG TCCTTGTTAA TGGTAATGAT GTTATTTGCA ATTACATCTA GTAACCCTAC 180 ATCCGTTGGT TTTAGTAGTA GTATTTGATT GTAAAGTTGC AGAGCCTCCT CTGTTTGACC 240 CTGAAGCTGC AGAATATAGG CCATCTGACC ATAAGTGATG GCCAGTCCTG CCTGTGGGTC 300 TTCCTCAGTC TCATCAGTGT CTTCTGATAA TGAATGGTGG CAAAGACCTT CAGCTTTTTG 360 TAGGATGTTC ATGGCCTGGT TCAGCTGGCC GTGGTCTATC AGTGCACATG CAGTGTTTAG 420 CACAGCTCAT GTGTGCCTTC TTGGAAGCCC AGGCTCTCTG GAGCCACTTT TTCCCAATTG 480 CTTTGAGCTG CAACAACTGC TGAAGGGTTT GTTTTCCTCT CCTCATCATA AGCATCGTGG 540 GAGTTTCGGA CGAGATCTCT TTATGCCACT AAGCATTCAT CATAGTGTTC CAAACGGTGT 600 AACACTTATC CATAAAGCTC CTTCAGTTTG TCTGTCTGCC GGTTGGTACT TTCTACTGTC 660 TTCAAGACAT TCTCAATTCT GTTGAGCCTG TACTCGCAAT ATGCCTTTTC AAAGGAGAGA 720 GAGTTATTGG CTAACAGTTT GGTGCAAGTA TTGATGACAT TCAAGGCTTC TCTGAAACTT 780 CCTTTCTGGA TAAGGCATAT CACTTTACAA TGCAGGCCAG TTACATCATC TTTGTGGATC 840 TGCAGTATCT TATTGACAGG CTTGAGAGCA CACAGGAAGT TGCTGTTCTG GCCGTACCGG 900 TTCACTTCAC TCCACACAGC ACAGGCACTG AAACTCCACC CTGCTGCTCA CTGTCGCCCA 960 GGCTGGAGTG CAGTGGCGCA ATCTTGGCTC ACTGCAACCT TCGCCTCCCG GGTTCAAGTG 1020 ATTCTCCTTG CCCCAGCTTC CCAAGTAGCT GGGATTACAG GTGCCCACCA CAACACCCGG 1080 CTAATTTTTT TGTTGTTTTT AGTAGAGACA GGGTTTCACT ATGTTGGCTA GGCTGGTCTC 1140 GAACTCCTGA CTTCGTGATC CGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTGCAGACGT 1200 GAGCCACCGC ACCCGGCCTA TCATGGAAAT TTTAAAACAT TGCTAACAGT GGAGACTGGT 1260 GTAATAAAGC ACTGTATCTT GCCCAGCTTT GGCAATTTTA AAACGTTACC AGTTTTGTTT 1320 GAGCAATACC TCTCACGTCC CTCCACTTGG ATTATTTTAA AGCAAATCAA GCTGTCATAT 1380 AATTTTGTCT 1390
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