Tag | Content |
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EnhancerAtlas ID | HS095-22191 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr4:9605250-9606740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF8 | MA0652.1 | chr4:9606544-9606558 | CCGAAAACGAAACC | + | 6.14 | IRF9 | MA0653.1 | chr4:9606543-9606558 | ACCGAAAACGAAACC | + | 6.66 | RFX2 | MA0600.2 | chr4:9605756-9605772 | TGTTACCATGGAGACA | + | 6.03 |
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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 |
GH04I009602 | chr4 | 9603949 | 9607947 |
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Enhancer Sequence | TAAAAGCCAA GGAGTTGCTA AAGACGTGTT TACTCAGACT CTAAGACCCT AAAGACGCCC 60 AGTGGCCTAT TTATCTAAGA GGCTAGATCC TGTGGCCTCT AGATGGCCAA GTTGTCTGCG 120 AGCCATAGCG GCTACAGCAA GCCTAGTCCA AGAAGATGGT AAGTTAACTG TAAGCCAAAA 180 TTTAACCCTT ACAGCTCTTC AAGCCATAAA GACCTTACTA CGAAGTGCTT CTGGCAAATA 240 GATGTCAAAT GCTCGCATCT TACAGTATCA AAGTTTACTG TTAGATCAGC CTCGTTTGAC 300 TTTCTCTCCC ACAAAGTGTT TCAATCCAGC TACACTACTT CCCGACTCAG ACTGCACTAT 360 TCCTGCTCAT GACTGTCAAG AACTGTTAGA AACTATCGAA ACTGGCCAAT CTGATCTTCA 420 AGCTGTGCCC CTAGAAAAGG CAGATGCCGC CGTGTTCACA GAAGTAGCAG CTTCCTCAAG 480 CAGGAAGTAG GAAAAGCCAG TGCAGTTGTT ACCATGGAGA CAGATGTGTT GTAAGCTCAA 540 GCTTTACCAG CGAACACCTC AGCACAAAAG GCTGAATTGA TCGCCCTCAC TCAGGCTCTC 600 CGATAAAGAG TAAACGTATT AACATTTACA CTGACAGCAA GTACGCCTTT GCTACTGTGC 660 ATGTACATAA AGCCATCTAC CAGGAAAGCA GGCTACTCAC CTCAGCAGCT AGCTGTGATC 720 CACTGCAAAG GACATCAAAA AGAAAACACG GCCGTAGCCC ATAGTAACCA GAAAGCTGAT 780 TCAGCAGCTC AGGTCGCAGC AAGACTTTCA GTCACGCCTC TAAACTTGCT GCCCACAGTC 840 TCCTTTCCAC AGCCAGATCT GCCTGACAAT CCCGTATACT CAACAACAAC AAAAAAACTG 900 GCTTCAGATC TCAGAGCCAA TACAAATCAG GAAAGTTAGT AGATTCTTCC TGACTCTAGA 960 ATCTTCACAC CCTGAACTCT TAAAGAAACT TTAATCAGCC ACCTACAGTC TACCACCCAC 1020 TTAAAAAGAG CAAAGCTACC TCAGCTCCTC CGGAGCCATT TTAAGATCCC CCGTCTTCAA 1080 AGCCTAACAG ATTAAGCAGC TCTCAAGTGC ACAACCTGCG CCCACGTAAA AGCCAAACAA 1140 AGTCCTAAAC CCAGCCCAGG CCACTGTCTC TGAAAAAACT CGTCAAGAAA AAAGTAAGAA 1200 ATTGACTTTA CAGAAGTCAA ACCATACCAG GTTAAGGACA AATACCTTCT AGTACTAGTA 1260 GACACCTTCT CCAGATCGAC TAAGGCATTT GCTACCGAAA ACGAAACCAC CAACACAGTA 1320 GTTAAGTTTT TACTCAATGA AATCATCCCT CAATATAGGC TGCCTGCTGC CATAAAGTCT 1380 GATAATAGAG CAGCCTTCAC CTCACCTATA GCTCAGTCAG TCAGTAAGGC GTTAAACATT 1440 CAATAGAAAC TCCATTGTGC CTATCAACCT CAGAGCTCCA GGCAAGTAGA 1490
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