Tag | Content |
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EnhancerAtlas ID | HS095-19371 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr22:19086000-19087380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr22:19087265-19087280 | AAGGTCAGGAGTTCA | + | 6.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09763 | chr22:19084642-19087309 | CD14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 19086474 | 19087142 | chr22 | 19087169 | 19087223 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I019097 | chr22 | 19085478 | 19087306 |
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Enhancer Sequence | TAAAGCTTTA GCGAAAAACA AAAAAAAACA GTGGCCAGTT GCAGGTATAG TTTGCCAAAC 60 CCTGTTCTCG AGTATACATA TAGGGACATT TTACATACAT GTAAATGTTT TGTTTTTTGA 120 GACAGGGTCT CGCTCTGTCA CCCAGGCTGG AATGCAGCGG CATGACCACA GATTACTGCA 180 GCGTAGACAC CCTGGGCTCC AGTGATCCTC TTGCCCCAGA CTCCCAAGTA GCTGGGACTA 240 CAGGCACATA CCACCATACT CAGCTAATTT TTTATTTTTT ATTTTTAGTA AAGACAAGGT 300 CTTGCTATGT TGCCCAGGCT GGTCTCGAAC TCCTGAGCTC AAGCAATCTT CTCACCTTAT 360 GCTCTCAAAG TTTTGGGATT ACAGGCATGA GCCACTGTGT CTGGCTGAGG GACACATCTT 420 TATTGCTGCC CCATACTCCA TGTCACCAAC ACCCCACACA TGGAGGCATG CACTAAATGC 480 CTAATGAACT GCACAGCTCA AAATCTTCCC ATATTCTGCT AGCAGACAAT GAAGTGTCAG 540 AAGTTCTCCA ATAGGGAAGG TTTTTCTCCC TTCTTGATCC ATCTGTCAAG CCGGGTCTAT 600 TCTGGAAGCA ACTGAAGATG TGGATCACTC ATTAACACTG GCACCTACTC TGTGCCAGGC 660 AGTTCTCCAG GTGACAGGGC TGTGGTAATG AACAAAGAAA GTCAATTCCA GGACATGACA 720 GAGCTTGCAT CCAGCACAGC ACACCAGATG GTGACTCCAA CAGGTCAAAC TGGCATTGCT 780 TTAGCTGGAC ATCAACACTG CGTTTCCACT GACTACGCGT GGTGACTCAC GCCTGTTACC 840 CCAACACTTT GGGAGGCCAA GGCAGGTAGA TTACTTAAGC CCAGGAGTTC GAGACCAGCC 900 TGGCCAACAT GGTGAAATCC CAGCTCTACT AAAAATACAA AACATAAGCC AGATGTGGTG 960 GTGTGCATGC CTGTAGTCCC AGCTACTCAG GAGGCTGAGG TGGGAGAATC ACCTCAGCCT 1020 GAGAAGTCAA GACTGCAGTG AGTCACGATC ACACCACTGT ACTCCAACCT GTCTCAAAAA 1080 AACAAAACAC CACCACCAAC AAAAAATTGC CTGTCCTTTC TCAATATCCT CCACAGTCTC 1140 TCTGTAAAGC AGTAAGTGCA ACTTCTGCCA CATACAAAGT TGCTTAAAAA CAGTCACCCT 1200 TGGCCAGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGCACGTGG 1260 ATCACAAGGT CAGGAGTTCA AGACCAGCCT GGCCAAGATG GTGAAACCTT GACTCTACTA 1320 AAAATACAAA AAAATTAGCT GGGCATGGTG GCACATGTCT GTAATCCCAG CTACTCTGGA 1380
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