Tag | Content |
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EnhancerAtlas ID | HS030-14695 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr7:99274430-99276050 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr7:99275813-99275828 | AGACCACACACAGAG | + | 6.02 | RARA(var.2) | MA0730.1 | chr7:99275884-99275901 | TGCCCTTTGAGTGACCT | - | 7.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATTTCTACA GATTGACAAC TGTGTTCATG GCTTCTATTG GCCTTATAGA AATGTGGGCA 60 GCTTTCAGGT ACACCTCAGT CTCTGTGGTC AGATGATCTG GTTGATTTGA GCTGTTGAGG 120 AGGATGGTTG ATCCATATGT CCTTGAATGA TTGTGTGCAG AAGAACCAGC AACTAATACT 180 TCTCAGGTCA TACTCACCTG AGAAGCACAG TGCCAGGCAC ACTCATCTTT TTCAAGGTGG 240 TCAACCAGAA AGCAGTCAGT TCACTGCCTC TGTACGTGAA GTATCTCTGA GGAAAAACCC 300 ATTAAGCCTG GTGTTCACTA TGGCAGGCCT GCCTGGAACT CATCTTTCAT GAGTCATGTG 360 CAAACTCCTC CAACTGATGG TTCTGGATCC TTGCAGACCT TCCCCCTCCG GTGTGACTGA 420 GGGATGGAAA ACTGGAGGAA GAAGAGAGGC TGAAGGAAGA GGTTGCCAGA CACTGATTCA 480 GCTGTGAAGC TGCTAGCCCC ACACAGTTGG CTCCAGAGAG GCAAACTACA AAAATGTGGC 540 TGAAAAAGAT GATGTGCATA AAAGAATCCA CATGCCTCAT ATGTACTTTC AGCTAAAAGA 600 CACAGAGGGA CCTTCCAAAG TCCAGGTACT TTCCTGTTGA TAGCAAATGG TGCAGTATGG 660 CATATAAGAT AAGTAATGAT AAAACGTCCC GGAGAGTTGT ATTAAGACCT TGTTTACTCC 720 TCTTTAGAGG TTAGCCTTCA AGGCAGTATA GGTTCCAAAC ATTTTGTAAA CATCCAGTGA 780 CTTATAAAAT GTGATAAAAT AAAACTGAGA AATTACATGA AGGGCAGGGT TTGGAGGACT 840 CAGCAGGGGC AGCATGAGCA GGCCCAGTCA TACATTTGGT TCCCTGCCCC AGAACAGTTA 900 GTGGAAGTGC GTGCACCACC TGCCAAAGCC AGGGTGGCCT TGGGTATTCC CACTTCAGTT 960 CCCTCCTTTG TTGTCACAGC CATGTCAAAT CAATGACACT AATCTCTGCT CCTGAACTTT 1020 AAACACATTA CCTGACCTCT CAGGTGAGGA CAAGCTATTG AGTTAATGTG TCAGCAGCAT 1080 TGGCCCCCAA GGAAAGATCT TGGTGAGTGT CTAGATTCAC ATGGTACCAT GTCAAGGCAG 1140 ATGCTGTGCT GGGCGAACTC TTTAGTTTCT TTCCAGCTCC CCTCTGGTAG AGTAATGCAG 1200 CCTTTGGGTC CAGTGAAGAG ACTAACAGAA AAGCCAGTCA TCTATTGCAT GTAATTGTGT 1260 TGGCCTAAGG AGGGCCTGGT CTACACTGCA TTTTCTGACT CCTGGGCTGC ACCAGCATTG 1320 TCTAAGGCTA AGGCATTGTC TGCCTGGCTG CCCGAGTCTG TAGTGACCGG CCCACAACAT 1380 GGCAGACCAC ACACAGAGTG ACACAGATGG TGCCCCTGTG TCCAGGCTTG AAGCAGATGA 1440 GATGCCAACC TGTTTGCCCT TTGAGTGACC TCCACGGTGG GGCCAGGACC CATGAATATC 1500 TCTTTGGAGT TCTACCCTGA GAGCTGAGGA ATATTTTCTC ACTTCATATG GATCCTACCT 1560 GGAAGCCTTT GCTATCGTCA CTGGCTCACA GTCTTGCTTA CTCCCCTGTC CTGAGAGTTT 1620
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