Tag | Content |
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EnhancerAtlas ID | HS047-31829 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:139929380-139930370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr7:139929412-139929427 | GGTGACCTTGGACTG | - | 6.06 | PLAG1 | MA0163.1 | chr7:139930242-139930256 | CCCCCGTGGTCCCC | - | 6.15 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_10688 | chr7:139928670-139933684 | CD19_Primary | SE_23582 | chr7:139928853-139932390 | Colon_Crypt_1 | SE_23882 | chr7:139929232-139932362 | Colon_Crypt_2 | SE_32404 | chr7:139929315-139932427 | Gastric | SE_35628 | chr7:139928783-139932537 | HepG2 | SE_50458 | chr7:139928716-139934014 | Sigmoid_Colon | SE_52813 | chr7:139928906-139934034 | Small_Intestine | SE_58244 | chr7:139929339-139931797 | VACO_9m | SE_63142 | chr7:139906757-139942538 | Tonsil |
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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 |
GH07I140229 | chr7 | 139928803 | 139934470 |
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Enhancer Sequence | AATCTGCCCT TCAGTATGTC CATCCTGGTG GAGGTGACCT TGGACTGGCG TTTGACTCCC 60 CACAGCCAGT CTCTGCTAAG CCCTGTCACC ACATCAAAGG GGCCACCTAG ACAACGTGAA 120 GTCAGAGGAA CCCCAATCCT GCCCACACTT CAAAGGGGCT CCTCTTCCGG AAGTTGTTAC 180 AGCATTCCTT TCAAGGAGGG TAAACAACGA AACAGCTCCA GGAGCTCACA GCTCGCTCCA 240 GCTACATCAC TGGCCTCCAC GCTGGGACGT GGAGCTCTCT GGGGCCCAAA CAGCACACCG 300 AAGAATGAAA ATGTCCCTCT GCCGAGAGCA AGTCGGCCCT GCTGCCTTCC CATTTCACCC 360 TTCCACTAAT GAGCACCAGG AAGCGCCCCT CCCAGGGCGC GCCCTCAATC AGCGTCTGGC 420 CCTGAGCAGG TGGCACCCCT CTCTTCCTCT CTGCCCTCTG TCAAGACCAT ACCACGGCTG 480 TTTTGACTCC TGGGCTTCCG CCCTTTAGTT TACACATTTG ATGATTCCGT TTGAAAATCG 540 CAACCTGAAA TACTCCTCTT CTAGGCTGGA GGCGGGGTTG GGGGCGGGGG CGGTGGGTGG 600 CGGAAGGAGG GCCCTCAAAC AAAGATCCGC TTTCTCCTGA ACAGGTGTCA GGAGACCAAG 660 CTTTGACCTC CAGCTCCCTG GCCTCCGGGC GCGGGCCCTG GGCTGATCTG GCGGTGGACG 720 TGCAGGGCAG CGGGCCCGCG CCCACCAGCT GTGGCAAGTT TCTAGTAAGA GAGGGATAGA 780 GACAGGCGGA GACCGCTGGG GAGTTTCCCG GTGCTCAGCC ATCGCATAGG GGGGAACGGA 840 CCCTTTTGTG GGCCCTCGGG TCCCCCCGTG GTCCCCGCTG GCGCGCTCGT CCTCTGCCAC 900 CCCCAGATCT CTGCGCACTC CCCACTCCTG GGCGTTCGCA CTGCCCCCCG GCGCACTCTC 960 GCCGCCCCGG GGTCCGAAGC ACCGCGCACT 990
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