Tag | Content |
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EnhancerAtlas ID | HS052-29301 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr4:147112570-147114080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr4:147113474-147113489 | TGACCTTTGTCCTCC | - | 6.14 | Nr2f6 | MA0677.1 | chr4:147113474-147113488 | TGACCTTTGTCCTC | - | 6.35 | RARA(var.2) | MA0730.1 | chr4:147113388-147113405 | TGACTCTTGGGTGACCT | - | 6.39 | Rxra | MA0512.2 | chr4:147113474-147113488 | TGACCTTTGTCCTC | - | 6.19 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I146191 | chr4 | 147113031 | 147114027 |
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Enhancer Sequence | GTTTAATAGC TCTACAGTGG AGTACTGTTT TCAACCATGG AACTACTTTT AATCAAGATC 60 AACTTTGGGA AGTGCTGCCA TTTTTATGGT AATAAAGGAC TGTATTATGC ACTTGAACCC 120 GCTCAAGTTG TCCCCTGTGT ATACCTTCAC ATAGTAGAAC CATGAAACAA AGTGTAAATG 180 CTTAAATTGC TTTGTTCTTA ACTGTAGTCT CCTAGAGGTC AGTGAATGAT TTCTAGTTGC 240 ATTGTAGCGA AGACATTTGT TCCAGGTTGA AGAATTTTTT ACTTGAGAAC ATACATTTTC 300 CCTGTCTGTG TGCCCCCAAA CCCTGTCTGC CACACTCTTT CTCTTGGGCT GTGACAAAAC 360 AGAATGTTTA GCGAGAAACA AAATTGTGCT CGATTTTCAG ACTATCTGAC TTCATTTTCT 420 GTTTTGGTCT TTGAGCTATT CCTTGGCTAA TCTTCCAACA AGTCGAATTG ATTCTTATTT 480 CAAAACTGTT TATCCCAAAA CAGAGCTGTT GACAAGTACA AATACAGATG GCAGACATGT 540 GGTATGATTT TCATGTTCTC ATCTCAGCAT TCAGGAAGGG AATGTTATTG AAAGATGGTT 600 TACATCTGAA GCTTTCTGCT CAAGGCAATA TGGAATGCAT GCTAGGAGCG CTTAATTATG 660 CTTAATTAAT AATAGTAACA AATGCTTACG GGATTTCCTT AAGGTCTAAA AGTGCAGCAG 720 CATTGGACTT GCTGTGTAAG GCTTACCGCC CCGGAGGCTA TAATAATCTG TAACAATAGA 780 AGCAACCTCT AGGGGGTAAA ATTGTCTTTG ATAATCACTG ACTCTTGGGT GACCTCAGTA 840 CAGCATTCCA GGCCAAAGAT CCAGAATGTT CCCTTACTGG GGGCAGACAC GCCTATGATT 900 GCACTGACCT TTGTCCTCCG AGCAGATGAT CCTCCAGAGT ACTGGCTAGC TCTTAGATTC 960 AGAGGTAAAT CCCAGCCCAT GCTGTGGCCT TGCTGTTCCC CACAGCCCAA CTGCATTAAC 1020 TATAATTTTT TTTTCTCCAC AAAAAGAAAT TGTTGGTGAA AGGAAGACAA CCTTCAGTTT 1080 TTCTCCCCAC CGACCTGGTT TCAGGAGGCC GTGTGCTCAG TGGAGTGTCT CTGCCTGTCT 1140 TCGCTAAGCT TGCCCCTGAC CATTGTGGAG GTAGATGCCA CCTAAGAGTG GCAGGGTTAG 1200 TCCTGACCTC TGGGGTCTGA ATATCCAGCA ACTATCTTAA TTCCAGTCGC TGCTGTCTGT 1260 TGTACCACCA GTACACAGCA GTACAGCTGT GTCTCTGTTG TTGACCGACT AACTTAGATT 1320 CACTGTTGAA GTCCAATTAG CCAGAGTGGG GGTGAAAATG CAAGAGTGGA CGGTGAGAGT 1380 GGTATGTGTC ATGTACGACA GGACAGTGGA GAGAGCCCTC TCTGATACCT GTTAGTCCCT 1440 CCTTTAAAAG ATGCGGGAGG TGGCCAGGGA GTGGGGATTT CAGAATGTGG TGGCAGAAAT 1500 CAGTTTGGCA 1510
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