Tag | Content |
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EnhancerAtlas ID | HS044-09078 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr3:79042440-79044680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr3:79043671-79043682 | AAATCTCAGCA | + | 6.32 |
| | 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 |
GH03I078992 | chr3 | 79041216 | 79045053 |
| Enhancer Sequence | GCATACTTTC AAAACGTTTC TTTAAAAATC CTACTTAACA AGCATACTCA AATCCTAAGT 60 AAACTGCATT GTAAGGAGAC CTTATTTTCC CCCTCATAGT TGTAAATTCC TTGAATTTGA 120 GTCAAATTTA GGCAGGAATA CAAAGGCCTA AAAGCCTGCA TTTACTCACT TCTTTATTTA 180 AGTGGAGGCA AGGGTGTAAT ACACTTATAT ATGTAGTTGA ACCCAGTCAA ATCAGTTCTT 240 AGACTTATTA GAGCATGACA CTGTTGACAC AAGGCTAAGT GAAAAGCCTT GACCTTTGCA 300 TTTCCGCCAT GACCTCAGGG ACTAGACCTC GTCATCTCAC CCCAACCTTT ACAACGTGAA 360 TCACACCAGA TCGGGTGGCT GTGTTTTTTG AAGGATCCAT TGGCCCAAAT GAAAACTATT 420 TACTTTGCCC ATAATTGTTA ATTCCTATGA GGCTTTTGCT GTGTTATTTA GTTTTCCAGG 480 GCTTCCAAAG TGAAATCTAT TCTACTTCTG TAAAAACAAG ATGTTCTCTA AATTCTTTAA 540 AGTTTGCATC AAAATCTGTT AAGCCAAAAT GGTTTTTTTT CCCACAAAAT CCTGTCACAT 600 TTTGACAGAA ATTCAAATCA AAGCAAAAGT TATGTGTAAA AAGGGTGTTA AATATTAAAG 660 GAAAAGAAAG AGAATGGTTA TTTTACTAGA TACCAGCTTT AAAAAAAAAA ATGACTAGGA 720 TGTTATAGTT CCCAGCACTT ACATGAAGTT TCTCATGAGA GGCCTCAACA AATCTAGTCA 780 TTTCAGCCAA ATTGATCTAT ATAGATATCA GACTTTATTT CTCATCTGCC TTTAAGATCA 840 ATATAGATAC AGAACAGAGT TTTAAAAGGA AGCTTTCGCC TTTTAATTCC ATTCCTGGAT 900 GGTCACAAGT AACCTTATGC CCTCAAACTC CATTCCTCGA CTGATATCCA GGCTCCAAGA 960 TTTGAATTCA ACCAGCGAAA AGGAAAGGGC TGTATCAGAT TACCCCAAGT ATTTACTGAG 1020 ATAAATGGTG AGGATGGAAG CATTTTGGGG GAAGCTGGAG CTATTAAAAA CAGTGGAGAA 1080 AAAAGGGCAA TTTTCTCCTC TAAATGTGCG CTACCATATT TTATGGAGGT AAACCACCTT 1140 CTTTATGTAA AAGATAGTAA ATCTGTTGAT GCCATTTGTT AGGATAGCGT TATCTTAACA 1200 AAGGGCATGA CATTCAGGGT TTAAAGTATT TAAATCTCAG CAATGTGAAA CACGGCTTTT 1260 AAAAGAACTT TCAATTGGAA ATACCGAGTA AATGGGTTCA CACAGCATGA ATTTTATTGT 1320 AGACCAACCT AATTTTCACA TTTTCCTCTC TAAAACAAGT GAGTCATTTG TTCTCTGTAC 1380 TCATAATGGA AAGAAAACAA GAGTTTCTTT GTTTGTGTAC ATTAACTCAA TGCTGTAAAA 1440 GTCATGCAGC CAAGCTTCAC TATACTTTCA CCTTTAAACC TTAACCTGAC TTGTAACAAT 1500 ATTTGTAGCC TCTAAAATTA CACTGGTTGA ACCCAGACGG AGTTAATCAC CCTTCACTGT 1560 CTCAGTGAAA AGTATAATGA CCTACCATTT AATGGGAGGC CATTAAAACG CTAGAAGGGG 1620 CAAGAATTCA CATCGTGTGT TTATACATAC CTCACAGACA TGAATCCATA CATTCAGCCT 1680 ACCAGGACAG TTTTCATATG GCACTTGCTT AGAGAACCAG ATGGAAACTA ATGACTGCTA 1740 TACACTCGAA GCCAGAAGTG TCTATTCTGC TGTCTTCTGT AGTGCACCTT ATACTTTTAA 1800 TACTGACAAA AATTAATTCT AACCAATTCC ATCTGTAACT GAACAAAGAA TAATCCAAAT 1860 CAAAGTTGGG TAACTGATGA TATTCTTTTC TTTCCGTAAC TACCGTTGCT TCCAACACAA 1920 GGCACATTCA TCGCCAGGAG CCTTGATTTC TACCTGCAAA GTATGTCCCA AATCCTGCCT 1980 TCAGGAATGC TACATTGCAC AAATCCAAAG GGTGATATCT TATCACTCAT GGTGCCTAGG 2040 CTTGCTCCAC AGGGTGGTTA ATGACGCCAG CAAGCATGAT GAACCTGGAA CCGAGCAACA 2100 CAGAGCCCTG CACTGCTTCT ATCCACCTCC CTGGCACCAT CTCAGACAGA GCCATTATCA 2160 AAGCCTTCTA AAGTGATCTC TTAAATCTCT GCCCCATCTC CACTCTTGCC TCTATAGCCC 2220 GTCGATCGGG AGCATGTTGG 2240
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