Tag | Content |
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EnhancerAtlas ID | HS078-04494 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr12:102799170-102800640 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr12:102799364-102799377 | AAATTAATTAACA | + | 6.19 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_00152 | chr12:102799548-102807365 | Adipose_Nuclei |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I102405 | chr12 | 102799549 | 102807365 |
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Enhancer Sequence | CTGCTTTCTT ATAGGAGTTC TCTAGAAAAA TGAGAGAAGG ACACATGGGG CCACAGAATA 60 GCATCCCTAA TGTTCCCAAA CTCCTTGAAA TGTTTTTGTT CAATTCTCAA TCAACACTGT 120 TGATGGTCTG TAGCTGATCA AACCCGCAAA ATAGATATTA TTAAGGATGC CATCTCTCTG 180 CCTAACTACT AACCAAATTA ATTAACAGGC GGAGAAACAC ACTAATTTGA ATTTTACCTT 240 TTGTTTTTCT GTTTAAGAGG CATACCAGCT CAAAATAAGA AGTTCTTTAA ACATCTGCAA 300 TGCCCAAACT AAGAAAATAT TCAGGAATGA AATGGGAACA AATTAAAAGA AAGCCTCATA 360 AAGCGTTTAA TCTCCATTCT TCCTCTCAAG CCAAATTAAT CCCAAATTTC TACAAGAAAA 420 CATTAAGATA CCATCTATGC TTCACTCTTT AAATTAGCGG GGGGCTATAG CAAAAAGAAT 480 TGAGGTTAGA TTGACCAACC ACATACATCC TATTTTTTGT CTCCAATAGA GAGATTCTTT 540 TTCTTTTCTC TCAAAGCACA AGGTATAAAG TGTAAAGTCT GAGCGGAGGG ATTCCCTGGT 600 CTGTTTCTTC TGGGTCTGTC TCAGCATCAC AGCAAAGCCA TGGGCTGAAA CTCACTTGAG 660 TGAAGCAGAT GCTGTACCAA GTAGCATGAT TCCCATGCAC ACACGTGCAC GGTGGAGGCC 720 ATTCAAACCA GCTGGGATAT CGTCTGGTTT GCATTTGGCT CTCTTCCCAG GCTGTCACAT 780 GTGACTTCTT TGTTGCAGAC AATGACAGTG ACAAAACAAA AGCACTCAGG GACTAGGTCT 840 CAGTTGCATC TGTTGCTTTG CTCATTGTCT TAACTTAATT ACGCCAGCCA CCCTTGACAA 900 TGGGCGGCAA GTGGAGGCAT GTTAGAAGCA GCCGTCATCA GAGCTGGCAC CCACCTTTGG 960 TGCACTTCTT GAAGAGTTAT GAAACTGTCT CACATTCAGT CAAGCAAAAA CTTTTCACTT 1020 CAGCAGCTTG TCCAATACAA ACAAACCAGC TGAAACTGTT TCTAGTATGC AACTAGACAG 1080 ATTTTTAAAA GGAAAACAGT AGTGAGTAAA TACTGTTTCC TATTGACACC AACGAAGGTA 1140 AGACTATTAA GAAAACATTG ATCCTCCAGC TCACTGGGGT TGGTTAAAGA AGTTTACCCT 1200 TTAGAAGGAA AGGTTAACAA ACACATTAGG AAATAAGTTT GTGGAGGGTT TGATTTGTGA 1260 TATATATGAT TACCCATTAT GGACAGACAC GCATATTTAG GGTGCTAGAA AAGGCCCTGA 1320 AGAGGCCATT CACCTTCTCC CATTATCTCT TGGTTCTTAT CCAAGCTCCA AGCTTTCCTT 1380 TGGAAAGCTA TCCACAGACT TTTCAATTAA GATTACTGTG CCAGGTGTGG TGGCTCACAC 1440 CTGTAATCCC AGCACTTTGG GAGGCCGAGG 1470
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