Tag | Content |
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EnhancerAtlas ID | HS095-22832 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr4:101210640-101212310 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr4:101211241-101211256 | TGACCTATTAATCTT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 101210670 | 101210914 | chr4 | 101211311 | 101211417 |
| | Number: 1 | ID | Chromosome | Start | End |
GH04I100288 | chr4 | 101209409 | 101212406 |
| Enhancer Sequence | AGTTGGCGGT GAGGGCCTGG AAAATGGGAA TTTTGGCTTG ATTTACATAT TTGGGCATCA 60 TCTGCACATG AGTACAATTT GGACAATATT ATCTAGGGAG AGTGATAGGA AAGGAAAGAG 120 AAGGACAAAG AAAAGGAAGT CAGAGTTTGG GCAAAGAATG AACCTGATAA TAGGAATGTC 180 AGGCATTTCC AGTGGAGATG CCACGGCTGA CTAGTAAGAA GCAGAGGTAA TCATGAGTGT 240 AAGGAGGCAA ATTAATGCCT ACTCCTTGGT TAACTGAAAA TAAGTGCTTA AATGCCTTTG 300 ATATTACTCT AAAGCAGTTA AACCTTGGTT AAGAAAAAGG TAGTGCACAA TTATAAGGTC 360 AGGAATTTAT GAACACTCAT TATAAGAGTG TAAGTTCAAA GTTTTCCTCA ATACAAAATG 420 AAAACCAGAA TAAGAGTAGC AATTATTTGG AGGTTAAAAA AACTTTAACT TATGCTTCAA 480 AGTTTGTAGT TTTGAACTGT ATTTTTATGT CTTTGCTGTG CCTATTCATT TGAAATGAGT 540 TTACTACATT CTTTATTTAT TAGTTATGCT TTTAAATAAA AATATGTTCT TGATTAGATC 600 ATGACCTATT AATCTTTCTT TCTCACTTCC ATACCTCAGG GACATCTACC CAGAAGATGT 660 TTACGATCAT AACTGAAGGG CTGAGCTTCC TGTCCATTTC CTCCCCTGCT TTTCCAGCTT 720 CACAGACAAC ATGCCCATGA CTTTTGAAGT TTTGCCAAGG GCTGTTCCAT GGGTGAAAAA 780 GATTGGTGAA ATGCTGTATT CCCTAAGAAT AAGTCAAAAC ACCACCCATT TTTCTTCCTC 840 TGTCTTCACA CTTTAGTATG TTAGGCTCCT GGGACATTTT GTTAGAGAAA TGTTCACTTA 900 GCAGATCACC ATCAACCGGC TATTGGCTGC AGGAATAACA GAGGCAATGC TTGAGAGAAG 960 TCACAGGTAT ACATGAGATT ACCCAGGGAG AGACAGCATT AAACATGCTA GTGTAAAATG 1020 TCACTCATCT GTGTGAATAT AACTTGCCCC TCTTCTAAAA GCAGTACTAA CCTGAATGAT 1080 TTCATCTGGA ATATTAATTT TCTTCAATTT CCCTGCCTAA TCAATCTGTC AGTTTGCATT 1140 TACCTTAAGA TCTTATGGCT TTTCTCAAAC TTAAGAGTTT AGGACACAGT CTTCTTCTAG 1200 GCATTTATCA AATGATTAAA TAAGGCTGAT TATTTGGAGA TCTGGCTGTT TACACCAGAG 1260 AAGGCTGATT CGCTAATCTT TTATTTCCTC TGTCTAAACT GCCTTATCAT CATCGGTAAA 1320 GCATCTTCTG ATTGCACAGT GAATTGGAAT GTTGGAGTTT AATTGTGGAG ACTCATGTGT 1380 CCAGGTGCTA GATAACATTC TACCTCACCT CCTTTGTTAG GAGCCCAGCA TCCTCATGTG 1440 CCTCAGGCTC CTTCCCTATA GTGGCATCCC ACATTTTGCT TTAGGTTCCT GACCTTTCCT 1500 TTCCACCTCT TTGAAAGTTT TGTACTCATT GTCACATAGT CACATGGCAA TTCATTGACA 1560 TTGGTGGCAG ACTGCTAATT TGATGAGCTA ATCACTGGAA TATATTACTG AGAGTGGCCA 1620 TCTTAATGGG CTTTTTTCTT GGTTGTGCCT TTTCTGTTAA TGGAGGCTAT 1670
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