Tag | Content |
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EnhancerAtlas ID | HS010-04213 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr7:106408420-106409270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr7:106408664-106408685 | TTTCACTTTCATTTTTCTGTT | + | 6.75 | IRF1 | MA0050.2 | chr7:106408658-106408679 | CTTCTGTTTCACTTTCATTTT | + | 8.79 | IRF2 | MA0051.1 | chr7:106408663-106408681 | GTTTCACTTTCATTTTTC | - | 6.38 | Myod1 | MA0499.1 | chr7:106408637-106408650 | TCCAGCTGTTCCT | + | 6.09 |
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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 |
GH07I106765 | chr7 | 106406261 | 106411934 |
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Enhancer Sequence | TGACCATGCC CTGTTAAATT AAGTTTAGCC TAAAGCTGCC TCCTTACATA TTTTTAAGTT 60 GAGGCTAAAG GTTTCTCTGC ACATAGTGAA CTGTAACCTA ACTGGATGTA TCAACAGACT 120 GTAACTTGCT CTTGTACCCA TCACTGAGCT TCAGCCAATT GCAGATGGCC AACTGTTTAA 180 ACCACGTTCA AATAAGACAA ACATCAAGCT GTAACAATCC AGCTGTTCCT ATTCCTCACT 240 TCTGTTTCAC TTTCATTTTT CTGTTCATAA ATCCTTTTCA CGTGAGTCTG TCTGAATCTA 300 TTCTGGTTTG GGGATTGCCC AGTTCATGAA ACATTCTTTG CTCAATTAAA CTCTGTTAAA 360 TTTAGTTTGT CCAAAATTTT TCTTTTAGCA GCTGCAGATC GCCCAACTCA TCGGTGGTAG 420 GTCTAAGACT CGAGCATGGG TCTTTAAGCC TAAAGTCTAT ATTCTTGCCA CATAGCCATG 480 CTATCTTCTG ATACATGTAG CAAAACTGCT ACAGAATTGG CCACCTGGAA CCAGTTAGTG 540 GTATCCTGCT ATTAACCACA TGTATTGGTT ACCTGATGCT GCCATAACAA ATCACCACAA 600 ACTAGGTGGC TTAAAACAAC AAAAAATTAT TATCTCAGTG TTGGCAGCTA GTAGTCTGCA 660 ACTAAGGTGC TGGCAGGTTG ATGTTTTCCT CTGACGCCTC TAGGGAACCT TCCTTGCCTC 720 TTCCTAGCCT CTAGCAGTTG CTTGCCACCC TTGGTGCTCC CTGGCTTCTA GATGCATCAC 780 TGCAGTCTCC ACCTACGATC TTCTCCCTGT CTGTGTCCCT GTGTCCCAAT GCTCCTCTTT 840 TTATAAGGAT 850
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