Tag | Content |
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EnhancerAtlas ID | HS007-12063 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr3:184291700-184293560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr3:184292620-184292635 | TGGCCTCTGCCCCCT | - | 6.05 | PLAG1 | MA0163.1 | chr3:184292916-184292930 | GGGGCCCAAGGGTA | + | 6.08 | RFX2 | MA0600.2 | chr3:184292595-184292611 | GGTTCCCATAGCAACC | + | 6.34 | RFX2 | MA0600.2 | chr3:184292595-184292611 | GGTTCCCATAGCAACC | - | 6.49 | RFX5 | MA0510.2 | chr3:184292595-184292611 | GGTTCCCATAGCAACC | - | 6.76 | RFX5 | MA0510.2 | chr3:184292595-184292611 | GGTTCCCATAGCAACC | + | 6.85 | SREBF1 | MA0595.1 | chr3:184292525-184292535 | GTGGGGTGAT | - | 6.02 | ZNF263 | MA0528.1 | chr3:184293060-184293081 | TCCTCCTCTCACCCGTCCTCA | - | 6.25 | Zfx | MA0146.2 | chr3:184291746-184291760 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH03I184574 | chr3 | 184292122 | 184293070 |
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Enhancer Sequence | CCATGTTGGT CAGGCTGGTC TCGAACTCCT GACCTCAAGT GATCCACCCG CCTCGGCCTC 60 CCAAAGCGTT GGGATTACAG GTGTAAGCCA CCACTCCTGG CCCTGGGCAA GTTACTTAAC 120 TGTTTGAACC TTGGTTTCCT TATGTGCAAG ATGAGGAAAA TAATAGAGGT TCCTTCATAG 180 GGCTGTAGCG AGGCTTCTTA TGTGAGCAAT GCTTTGCCCG TAGAACAGTG TCTGGCACAT 240 GGGAGCACAG CCACCAGCTA AGTGTTGGCC ATGAGTCTCC AGAGCCCTGG CATCCACGAG 300 AGCTGGGCTG TTCTGCCCTT ATTGTATACA TGAGGAGTTC AGGAAGCCTG CCTCGGATGG 360 CTTGCCAAGA CTTATGTACT AGGCTTCGGA GTTATCAAAA TTGTCCACCT AGGGGGTCTC 420 TCACTGAGCC TCACCAGTCC TTGTGAGGTA GATTCCTGCC ATCTCCCTAT TTCGCCAATA 480 AGGAAACTGA GTCTTGGAGA AGCTCTGTGC ACAGGCCTTG TAGCTAGGGA ATGTGGAAGC 540 TGGCACGGAA GCCTCCTCCT GTGCTCTGCC ATGCAGGATG GCATGCTGAG GGCCCTGTCT 600 TTCGCTCCCT CTGCCCGATT CTCTTCCTTG GGGCTTGCAG CCTACAGCTC TGAGGGGTAG 660 GTGATGACTC TTATGGCAGC CCTAGGCGTG AGAGGGGCTT GGCAGCATGA AGCTGGCTGC 720 GAGGCCATGT TGTCATGAGA AGGTGAACAG TGCCTTTCCC GGGCCCTCTC CACTTCTCGA 780 TGGGAATCTG TCCTGAGATT TCCTCTTCCT AAGTGGAGAA AGGGGGTGGG GTGATGAGCC 840 TGACAGCCTG AAGAGGGGCT AACACTCTGC AGGTCCCCGG CAGGAAATGC ATGCTGGTTC 900 CCATAGCAAC CAGGCTGGCC TGGCCTCTGC CCCCTCCCCC ACTGGCTCAA AAGAGCTAGG 960 GTGGAATATC ACCTTCGTGA GGGCAGATGA AACCCCAGAA AAGGGCAAGC CCTAGCGCTG 1020 GGCGTTCTCC CCTATGGGTG TCCCCCTCCA CAGGCAGTCA TATGGAGAGG CAGTGACCCA 1080 CTTTAGTGTC TAGGAGGGTC TTGGTTTATG CCCATTATCC TAACACAGTT ATTACTAGTG 1140 CCTCCTTTGA CTTGCAAATG TTCCAGTGTG AAGAATACAC GATAAGGCTA CCATCAATCC 1200 ACAGAGCCTG TGTCCAGGGG CCCAAGGGTA GATGGCAGGA GGGAAGACTG GGGAGAAGGG 1260 ATGCTCAGGC CCTGGGCTTG CTCTGGGGTG AGTCCCCTTG TGGACACTTG AGGCCTCTGA 1320 ACTCCAGGTG ACCCCAGCCT TCCTGCCTGC TTTCTTTCTC TCCTCCTCTC ACCCGTCCTC 1380 AGCCCCCATC CCTGCCCAAG GGCAGACAGG AGCTGCTGCC TGCGCCTGGT GGGTGGGGCG 1440 AGAGCTTCAC TGTGAAGGTC CCGTCTCCTG GCTGTTCTAG GGTGTCCTTC AGGGTCCTCA 1500 GGAATGATTT TTCTGGAGCC TCGGGGAGAG GTGGGGCATC TCCACAGTGC CGGGTGCTGC 1560 TAGCCCACCG GTGGTCTCTT CTTCACCCCA CCTCTTCCTC TGTCTTTCTC TGTCTTCCCT 1620 GCCTCAACAA GCCCAGGCTG TCCAGGTGAT GGGGCTGACG TCTTCGTCCA TGAGGCCCCG 1680 GGGTAGGGGT GAGGGGGGCA GGGGCGGGGA GGAATCTGCT GACGTGGGGT TTCCATGGGG 1740 CAATAGGGCC TTTTGTAGCT GCAGCTGGAG TTAGGCAATC CCAGCATTGC CCCCACAGTC 1800 TAGGAGGTGG AGGGGCCAGA CCTAGGCTGG GGAGAAGCCA GGTTCTCATG GAGCTGCGGA 1860
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