Tag | Content |
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EnhancerAtlas ID | HS129-36955 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr9:33133190-33134340 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RORA | MA0071.1 | chr9:33134226-33134236 | TGACCTTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_10912 | chr9:33119344-33169982 | CD20 | SE_27770 | chr9:33133434-33136209 | Fetal_Intestine | SE_28724 | chr9:33133427-33136185 | Fetal_Intestine_Large | SE_31534 | chr9:33133555-33134361 | Gastric | SE_42236 | chr9:33133177-33134351 | Lung | SE_48426 | chr9:33133123-33134192 | Psoas_Muscle | SE_58985 | chr9:33124740-33168862 | Ly3 | SE_62118 | chr9:33106994-33169093 | Toledo | SE_62346 | chr9:33106942-33169226 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr9 | 33133280 | 33133507 | chr9 | 33133730 | 33133860 | chr9 | 33134150 | 33134329 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I033133 | chr9 | 33133697 | 33146567 |
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Enhancer Sequence | GCGCCTAGGC CCAAATATAT ATTTTAACCT ACCTATATGG CACCCAGACC ACAGCTGTCT 60 GTCTTCTACT CAGGCAGATT TGTGGGATGC TATCAGATGC CCTGCTGAAT AAGATATGAC 120 AGCATTGTAT CCACAGTACA TCCCTCATCT ACTGGCATAG CAACTGTCAA GAGAGAAACG 180 AGATGCAGCT GGCACGGCTT ATTAGTCATC CCTGCTGGCT CCTGGTGATG GTGGCCGCCT 240 CTTCCAGGTG CTCGCTGCCA CTGCTTTAAT AACAGGCTCC TGAATCTTGC CGTCATTGGT 300 ATGTGCTAAC TGGCATCAGA CAAATGTTTC TCAATCACAG AGCTTTTCTT AAATGAATAT 360 GTGTTGGGTT AAAGTGACCC GCATTTTGCA GGACATTTAC CTGTTCTCTC TTGCATTCTC 420 CAATATTCTT CCAAGGTGAC CCACAACTGC GTGGCTGTCT TGCTTGCAGG TGTTCATAGG 480 GCCCTGGTCT GTACCTCACT TGGCCGAAGA ATTCAAACAG CCTCAAGGGG TTTGCCCACC 540 ACCTGCTCTC CTGCTTCAGT TTCCTTGTAA CAGGGCTTGT TCTGCTCTCT CCTGCCTCAC 600 AGGCTTAACT CTGACACCTG GTCCCAGAGC TTCTGGTGCT TTCCTACCCC AGTGGGCATC 660 TCAATTTCCA GGAACATGCA AGGCTCCTTT CTGCCTTAAG GTCCCTGCTC ACTGGCCCCA 720 GCTGAGAAGC CCATCTCCCT GCAGACTTTA GAACCTAGTT TATATCCTGG TTCTTCCAAG 780 CCATTGCTCT CTCTCCTTCC TCTGAGCTTC CAAAGCATTT GGCAGCCACC ATCCAATCAC 840 AGGATATTTG GGTCTGTTAA CAAATTGTTC CCTGGGAAGG TCCCACTTGC CAGAAGTGGG 900 TTGGAGGCTT CGGGACAGGG CAGGACTGAG ACCTTACACT TCTTCAGAAT CTCCCTGCAG 960 CAAGTGATGC AGCACAATGC CACAGCAGTC CTCGAGTGCT TCCCCTGGGG TCATAGGGAA 1020 GGTGCACAGA GTTCCTTGAC CTTGATGGAA GCCGTAAACT GCCAACAATC CTCCTACCTA 1080 AAGCAGAGTT TATCTCGAAA TGAAATGGAC ATTGGGCCTT GTAGAAATGG GCGTACTCAG 1140 ACTCTTCAAA 1150
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