Tag | Content |
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EnhancerAtlas ID | HS130-00029 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr1:1619670-1620850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:1620614-1620626 | AAACAAACAAAC | - | 6.32 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_13835 | chr1:1620449-1621388 | CD34_Primary_RO01536 | SE_27558 | chr1:1619469-1620436 | Esophagus | SE_45385 | chr1:1619731-1620531 | NHLF | SE_50179 | chr1:1619812-1620438 | Sigmoid_Colon | SE_65325 | chr1:1619810-1620683 | Pancreatic_islets |
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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 |
GH01I001688 | chr1 | 1619470 | 1621388 |
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Enhancer Sequence | ATGAGAAGCC ACCATCTGGC CACCATCACG ATCATCATCA CAATCACGAC GAGTCACCAA 60 GAGACTAAAA CTACTGAGTA AAAGCTTAGA AACGGCCGGG CGCGCTGGCT CACACCTGCC 120 ATCCCAGCAC TTTGGGAGGC TGAGGTGGGC GGATCACAAG GTCAGGACAT CGAGATCCTC 180 CTGGCCAACA CAGTCAAACC CCATTTCTAC TACAAAAAAT TAGCCGGGCA TGATGGCGCG 240 TGCCTGTAAT CCCAGCTACT CAGGAGGCTG AGCCAGGAGA ATCGCTTGAA CCCAGGAGGT 300 GGAGGCTGCA GTGAGCGGAG ATCGCGCCAT TGCACTCCAG CCTGGGCGGC AGAGCGAAAC 360 TCTGTCCCAG AAAAAAATAA AGCTTAGAAA CAAGAGGCTA TGTAGTCTCG AGATAGATCC 420 AGCCCTATGA GGCACATGTC AATCACAGAG GGAAAGCTAT GCACGCACAA AGCATGTGTG 480 AATCAGAGAG AAAGCTATGC ACGCACGATG AGTAGAAGAC AAACACGTCC TGCAAGGAGA 540 CGGAGGCGCA GGGAGGGGGC GGCAGCCGTC CTCCCAAGAC ATGAGGACTT CTAGTTCAGT 600 CTGAGACCTT GGTGCAGGGC TGGGCGAGTA AACAAATGCA AAAGAATAAG GACCTCGAGG 660 TCGGGCGCGG TGGCTCAAGC CTGTAATCCC AGCACTTTGG GAGGCCGAGG TGGGCGCATC 720 ACGAGGTCAG GAGATTGAGA CCATCCTGGC TAACACAGTG AAACCCCGTC TCTACCAAAA 780 ATACAAAAAA CTTAGCTGGA CGTGGTGGTG GGTGCCAGTA GTCCCAACTA CACAGGAGGC 840 TGAGGCACGA GGATCACTTG AACCTGGGAG ACGGAGGCTT TAGTGAGCTG AGATTGCACC 900 ACTACACTCC AACCTGGCTG ACAGAGCGAG ACTGTCTCAA AAAAAAACAA ACAAACAGGT 960 CTGGTGTACC CAGAATGGAG GCACCACGAG TTGCTGAAGA AGGAAACTTT ATTCAGTCTA 1020 TGATACCAGG ACAGTTGTCC ATGCTGCCAG GCAAAAAGAA AAACTGGATT CTGATCTCAT 1080 TATCAGTACA CAAACAGCGA CAATTAGTAA CACTGACACA GCCCTGACTG TGCTGCTGGA 1140 GGGTCCGAAG CACTCTCTGC ACAGCGGTGA ATCCCCACAA 1180
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