Tag | Content |
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EnhancerAtlas ID | HS059-04333 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr1:226951240-226953300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr1:226952699-226952710 | TATGCCAAGTA | - | 6.14 |
| | 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 |
GH01I226763 | chr1 | 226951083 | 226953262 |
| Enhancer Sequence | TCAAGTGATT CTCCTGCCTC AGCCTCCACT GCACTCCAGC CTGGCAAGAG AGCAAGACTC 60 CGTCTCAAAA ATAAATAAAT AAATTGTAGA GACAAGGTCT CACTCTGTTG CCCAGGCTAG 120 AATCAAACTC CTGGCCTCAG GCGATCCTCC CATCTTGGCC TCCCACAACA CTGAATTGCA 180 GGCATGACCC ACTGAAGCAA GCTCTTAATT AATTCCTATG ACAATGCCTA GGGATTGTGG 240 TGGTCAGTGT GCCCTTAGAG AATGAACTGG GAGATTCAGA ACGAAATCAT CACCCCAGCC 300 CCCAATAAGT CCAAGGATGT TGGATAGAGG GGTGCAGGTG GGGAACAGGG GTACCAAGGG 360 AGATCATGGA ATGTTTCCCC AGCCTGCAAT CTCCCCTCCT AACCAAGAAG AGAGCAGACG 420 CCATCTCAAA TCTCATGATT TATGTTGATG TCATTGTTTC CAGACCCTGC GTCATCACAG 480 AGGGTAACCT TCCCAGGCTC TTCCTTCGGG CTACTGTCTG ACACTCAGCA TTTCCTGCTG 540 GTGCTTGTCT GCCCCCATCC CCCTTGGCTC TACTGGTTGA GCTATTCAAA TGCCTATGTA 600 GGTTCTGCTG AATTTTCAGA ACTTCACATG ACTCATCCCA TGCATTTCAG TGACTGCAAA 660 GAAAAGTAAA CCATTCCCGC TGCTAAAGAC AGTTGTCTTT ATGCTTACTG AGATTATATA 720 AATCTGCATT TTATTTTTGC AACTTCGCAA AGAAACATTT GATGGGGGAG TAATGAGGGT 780 AAGGGCAGGA TGGGGAATAA GGTGAAACAG AAGTTACATT GCGCACAAAT GCGACATGCA 840 TCTGCAGATC TTTTTTTGAT TTATTTCTAA AAACATTTTC TGGGACCTGG AGCCTCATGC 900 AACCAGATTT CTTTGCCTGT GACCCCTCTT CTACTTTAAA TATGGATCAG TACCTCACTT 960 CTCTGCCCCA TTCTCTTGTC TTCTCTACTC TTCTAATTCC ACTGCTTCAG CCTCTACCTT 1020 TGCTGATGCC TCCCCAAACT GCCCAGCTCT CTTCTCTCCT GAACATCAGC CTTGTGTTTA 1080 AGACAGCCCA ATGTTACCAA AGCCAGCAAG TCCAAATTAA ACCCAGTATG ATTGGCCCCT 1140 TTGGTGTTTC GATTCTCAGT GAAGGACCTA ACCACAACAC CTGTTCATCA AGCTACAAAC 1200 CCCAGAATCT TCAGTTTATC TTAAGAGTCT GGCTTTCCTT CTTATTCACT GTTCCTCACT 1260 CCACCTGAGT TAGCAAGCTC TCTCCATTCT ACTCCAACTT CCAATGTGCC TCAAAGTCAC 1320 CACTTCCTCT CCACTGCTGC CCCACTGCTT AGACCCACAC TATCCCTGCT TGAACTACGG 1380 TGAAAGCCTC CTCATCAATT TCTTTGCTTC TTCATCCATC CACTCATCTG TCCTTCACAT 1440 ACTTATTGAG CACCTGCAAT ATGCCAAGTA CTGTTTTAGC ATCCAGAGAC ACAGGAACAA 1500 AACAAACCAA CAAGACCCCT GCCCTCATGA AATTTACATT CTAGTGAGGT AGCCAGATAA 1560 CATACAATAA ATAAAGAACT TCCTACCTAA GATGGCAGTT TGAAATTTTC TCACAGAGTT 1620 TGATATGGTT TGGCTCTGTG TCCCCACCCA AATCTTGTGT TGAATTATAA TTTCCGGTGT 1680 CAGAGGTGGG GCCTGGTGGT GGAGGTGATC GGATCATGAG GGTGGTTTCT AACGGTTTAT 1740 CACCATCCCC CATGTCCTGT CTCATGATAG AGTTCTCATG AGATCTGGTT GTTTGAAAGC 1800 GTGTAGCACC TCCCACTTTG CTCTCCCTCT CTCTCCTGCA GCCATGTGAA GACATACTTG 1860 CTTCTCCTTC ACCTTCTGCC GTGATTATAT GTTTCCTGAA ACTTCCCCAA CCATCCCTCC 1920 TGTACAGCCT GTGGAACTGT GAGTCAATTC AACCTCTTTT CTTTATAAAT TACCCAGTCT 1980 CAGGTAGTTC TTTATAGCAG TGTGAAAATG GACCAATACA GAGTTTTGGT CTGCCAATAC 2040 CTCAAAAATA GCCCAAAGAA 2060
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