Tag | Content |
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EnhancerAtlas ID | HS147-37870 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr7:24091990-24093420 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr7:24092180-24092192 | GTATGTTTGTTT | + | 6.37 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH07I024052 | chr7 | 24092012 | 24093250 |
| Enhancer Sequence | TTTCTACACA ATAGTTTTTG GGGTTATATA TGATTCCTAT TATAAGCTTC TTGACACAGT 60 TTTTGGAAGT AGATCATAAA TAAGTAAAGT AAATAAATAT GTGTATTGTG TTCAGATCCC 120 TGTCCTCTAG AAGGATTTTT CTACTGGATT TGTATTTGTT TCTAATATGT TTTACTTTAG 180 TGGCAATTTG GTATGTTTGT TTTATTTGCT TTTTCTGAGT TCTCTTATCT GTAGTGTGAT 240 TCCTTCTGAA TGGTGGGACA AACATTTGTG ACTATATTTC CAAACAGGTT ATTTGATGAG 300 TTATAAGGAC TTCAAAAATA TTCTCATTCC TTTTGACTTA GTACTTTAAA TTACAGCAAA 360 TGTTATTAAG GGCATTTTAG TGGGCATTCC AGGCATGATG CAAGGTTTTG GCAGGTGAAG 420 CAACTGGGCC ATAATAAAGC ACACTTGTCC CGACAGCCAT GTAAATAACA TTTGGGTTAC 480 ATGATGTGCT ATCTTTCTAT TACAAATGAC ATAAAGAATT GCTTTTCCGT ACATTGATTT 540 TTTTAAAATG AGGGTGTCTT GTATTGTCAG ATGGGGAATG TAGTTCTGAT AGCTCAAGTG 600 TTGTTGAATC AAGTAAAAAT CCCTCCCTGT GAAACTACAG GAAGTGAGTT GAAGACTGGA 660 GCCGAATGCG GCAGCTGCCT AAACCACTGA TGACTCATTG GCTAAATTGC GATTTAGTAA 720 TTTTGGTGTT GATAATTGGT AAGATAAGAT GACAAACCAA CCAGTCAGCT GCCTCAAGGG 780 TTTTAGTGAG TATAGCGGAG AATTCCAATT ACTTTCTAAG AGATCAGACT TCTCACTGGA 840 TGGCTTTTTC CCCTCTTGTT CTGATAAAGT ATGTTCTCTA CATGGCAAGA CAAGTGATGA 900 TTTTGTCACA TCTTCCTGGC TGGAGGTTAA GTTATATAGA TTTTTATGGT TTCTCTCTCT 960 GGGTTTTTGT ACTTTACTCC TGTAAACCAA AAGCACCTGC TTCTGACACT CCTACCATAC 1020 TCTTATCCAG GTCTGCTTTG AGGTTTTAGT TTCTCTCTTT CCTCTCTCCC TCTGTATTTG 1080 TGCCAACCTC AATGAATGAT AAATATTTTA GTAAAGATTT GGAAGGATAT GGGGGTTGGG 1140 GGTGCAAGGG ATTCTTACAT GGCATATCAT GCAACAAAAT CTCTAAATAT TCCCTTTACC 1200 CATCTCTTTC TTCAGTGTTT CTCTCCCTAC AGCAGATGTT CCATTTCTGT CACTTTCCAT 1260 CTTATCTTCC TGCTTCCTCT CCCACACCTT CTCCACATCT TCCTGTATTC CTCCAGGTAA 1320 CTCATTCTAA GTCTTCCTCT CCAGATGTTT CTATCGCACT ATCTTTTCTT GTGTAAAAGC 1380 AGCTTAACAC TCCCTGGGCA TCTGCAATAT GCATCCCTAT ATGTGCTGAG 1430
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