Tag | Content |
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EnhancerAtlas ID | HS191-33906 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr6:149610550-149611990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PBX1 | MA0070.1 | chr6:149610955-149610967 | ACATCAATCAAT | + | 6.44 | SCRT1 | MA0743.1 | chr6:149610643-149610658 | GCTCAACAGGTGTTT | + | 6.49 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I149290 | chr6 | 149611241 | 149611310 |
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Enhancer Sequence | TCCTTACCAT GGCCTAAAGT CCCTCATAGA TCACTGGGGA GACCTTTAAA GCCAGAGACT 60 GTGAGTCAGG GCCTGGGCTA GAGGCCTCTA AAAGCTCAAC AGGTGTTTCC CACATGCAGC 120 CACGTGGAGA ATCACAGTCC TGCCTGACCT GACCTCATTT TCCAACTCTC TCTTCACCCA 180 GTCCACTCCA GCCACTGGGC CCCTTGCTGG GCCTATGCCC GGAAACTACA CACCTCACTG 240 CTGTTGATGA AAAAAGTCAA ACTCTGTAAA ATATTTGAAA AGATTTATTC TGAGCCAAAT 300 ATGAGTAACC AATGGCCTGT GACACAACTC TCAGGAGGGC CTGAGAACAT GCGCCTAAGT 360 TGGTCGGGCT ACAACTTGGT TTTATACATT TTAGGAAGAC ATAAGACATC AATCAATGCA 420 TGTAAGATGG ACATTGGTTC TGTCCGGAAA GAAGGAACAA CTGGAAACAT GTGGGGTGTG 480 GGCGTGGGGG GCACAGTGGC AGCAGGGAGT TCCAGGTCAT AGGTGGTTGG CAGTTGGTTA 540 TTATCTAAAG ACCTGGAATC AAGAGAAAGG AATGTCTGGT CATGATAAGG GGTTGTGGAG 600 ACCAAGATTT TATCATGGAG ATGAAGCCTC CAGGTAGCAG GTTTCAGAGA GAAAAGATTG 660 TACATGTTTC TTATTAGACT TAAAAAGAGC CTGTTCTGTC AGTCTTAAGT TCTCTGTGTT 720 GATGTTAATG CTGGTCAGCT ATGAGGCATG TCCAACTTCC ACTTCCCACC ATGGCCTGAA 780 CTAGTTTTTC AGGTTAACTT TGGAATTCCC TTGTCTGAGA GGAGAAGTCC ATTCAGATGG 840 TGGAGAGGCT TAACACTGCT TTTGCAGGAA CCCATGGCTC ATCCCTCGCT CTTGCAGGTC 900 TTTGCTCAAA TGTCATCTTT TCAGAGGATG CATACCTAAC CACCCTCTGC ACCCTTCACC 960 CCGCACATTC TCTATTTTCC CTGTTTTTCT CAATAACAAT TATCACCATC CTATAGATTT 1020 ACTAATTTTT AATTATATTT CCTGCCCCAC TCTACTTCAC TAGAATGTAA ACTCCACAAA 1080 GGCAGAAATC CTTGTCCCTT CTGCTTTCCT ATATATCCCA ACAGACTAGA AGAGTGTGTG 1140 GTATTTAGGC TGGGCATGGT GGCTCACGCC TGTAATACCA GCACTCTGGG AGGCCAAGGT 1200 GGGTGGATTG CTTGAGCTCA GGAATTTGAG ACCAGCCTGG ACAACATGGC AAGATCCCGT 1260 CTCTACTAAA AAGACAAAAA AATAGCCAGG TGGGGTAGGG CACACCTGTG GTCCTAGCTA 1320 CTCAGGAGGC TCAGGTGGGA GGATGGCTTG AGCCTGGGAG GCAGAGGTTG CAGTGAGCTA 1380 AGATCGTGCC ACTGCACTCC AGCCTGGGCA ACAGGAGTGA AACCCTGTCT CAAAAACAAA 1440
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