Tag | Content |
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EnhancerAtlas ID | HS147-37335 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr6:158663060-158664240 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr6:158664062-158664076 | CCCGCCTCGGCCTC | + | 6.01 |
| | 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 |
| | Number: 1 | ID | Chromosome | Start | End |
GH06I158241 | chr6 | 158662918 | 158664315 |
| Enhancer Sequence | ATTACATCTA GTAACCCTAC ATCCGTTGGT TTTAGTAGTA GTATTTGATT GTAAAGTTGC 60 AGAGCCTCCT CTGTTTGACC CTGAAGCTGC AGAATATAGG CCATCTGACC ATAAGTGATG 120 GCCAGTCCTG CCTGTGGGTC TTCCTCAGTC TCATCAGTGT CTTCTGATAA TGAATGGTGG 180 CAAAGACCTT CAGCTTTTTG TAGGATGTTC ATGGCCTGGT TCAGCTGGCC GTGGTCTATC 240 AGTGCACATG CAGTGTTTAG CACAGCTCAT GTGTGCCTTC TTGGAAGCCC AGGCTCTCTG 300 GAGCCACTTT TTCCCAATTG CTTTGAGCTG CAACAACTGC TGAAGGGTTT GTTTTCCTCT 360 CCTCATCATA AGCATCGTGG GAGTTTCGGA CGAGATCTCT TTATGCCACT AAGCATTCAT 420 CATAGTGTTC CAAACGGTGT AACACTTATC CATAAAGCTC CTTCAGTTTG TCTGTCTGCC 480 GGTTGGTACT TTCTACTGTC TTCAAGACAT TCTCAATTCT GTTGAGCCTG TACTCGCAAT 540 ATGCCTTTTC AAAGGAGAGA GAGTTATTGG CTAACAGTTT GGTGCAAGTA TTGATGACAT 600 TCAAGGCTTC TCTGAAACTT CCTTTCTGGA TAAGGCATAT CACTTTACAA TGCAGGCCAG 660 TTACATCATC TTTGTGGATC TGCAGTATCT TATTGACAGG CTTGAGAGCA CACAGGAAGT 720 TGCTGTTCTG GCCGTACCGG TTCACTTCAC TCCACACAGC ACAGGCACTG AAACTCCACC 780 CTGCTGCTCA CTGTCGCCCA GGCTGGAGTG CAGTGGCGCA ATCTTGGCTC ACTGCAACCT 840 TCGCCTCCCG GGTTCAAGTG ATTCTCCTTG CCCCAGCTTC CCAAGTAGCT GGGATTACAG 900 GTGCCCACCA CAACACCCGG CTAATTTTTT TGTTGTTTTT AGTAGAGACA GGGTTTCACT 960 ATGTTGGCTA GGCTGGTCTC GAACTCCTGA CTTCGTGATC CGCCCGCCTC GGCCTCCCAA 1020 AGTGCTGGGA TTGCAGACGT GAGCCACCGC ACCCGGCCTA TCATGGAAAT TTTAAAACAT 1080 TGCTAACAGT GGAGACTGGT GTAATAAAGC ACTGTATCTT GCCCAGCTTT GGCAATTTTA 1140 AAACGTTACC AGTTTTGTTT GAGCAATACC TCTCACGTCC 1180
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