| Tag | Content |
|---|
EnhancerAtlas ID | HS070-01459 |
Organism | Homo sapiens |
Tissue/cell | GM19099 |
Coordinate | chr7:150132180-150133300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr7:150132472-150132488 | ACACTTTCTAGGAACT | + | 6.58 | | IRF8 | MA0652.1 | chr7:150132876-150132890 | AGTTTCGGTTTGGT | - | 6.04 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_59219 | chr7:150100493-150146824 | Ly3 | | SE_61492 | chr7:150097145-150147054 | Toledo |
|
| | 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 |
| GH07I150434 | chr7 | 150131890 | 150133736 |
|
Enhancer Sequence | CTGGGCTCAA CTCCTGGGCT CCAGTGATCC TCCCGCCTCA GCCTCACAAG TAGCTGGGAC 60
CATAGGTGTG AGCCACTGTG TTTGGCTGTA ATCGTTGTTA TTGTAGGCGC ATGTGCATGA 120
GGACCCTCCC TTCTTAGGCT CCTGACTCTA CTTTGCTTGG GTTTGAAACA AGTGACTCCA 180
TCTTGAAATG GACAACTGGC ACAGAATAGA GCATTTCAAG GGCAGATTAG ATGGCAACTT 240
AAAAAAAAGG TAAAGAAAAA TTAAAGAAAA AATTAAAGGT AAGGAAAAAT TTACACTTTC 300
TAGGAACTTC ACGAAGGAAG GGAAACATGA GACAAAGAAA GAGAAGTGGT TATCAGAAAC 360
TAAACTGCAC GAGGCTTGTG AGGTTTCTCA TGTTCCTCCT GGAACTTCCT CCTAGACTGT 420
ATTCTGCCAT CTGCTCTGGG GTCACGAGGG AAAGGGCCCC TCTCCTTTCA TGGCCTAGAA 480
AGCGTGGCTC TGAGCCATTC TTTGGGCTGA GGTGGGTGTC TGGGGTGCTG GTGGGGACAG 540
CCAGGCCCTG CCTTCCTGGG TACCTCTTGC TGCTTGTCAA CAGACCCTGC CCTCCATACT 600
GTGAGGGATT GAAGGATTAA CTCCAATTCT TTCCTGTCCT CCATTCATAC CCATGCCATT 660
GCTCATCTTG GGCGGACTGT ATTTCCCTGC CCATTGAGTT TCGGTTTGGT CTTGTGACTT 720
GCTTTGGCCA CTAGAATGGG GCAAAGTGAG AGGGTTCCCG TTCTCAGCCT GCCCCTTGTA 780
AGACCCTGCA GGCTTCTGCT GGCCTCCTGG GTTTCTGCCC TTGCCTGGGG GCTTTCCCTG 840
GGTGGTTTCG GTTCCTTCTA CTTGGTACCT GAAATGAAGA CATGTGGGAC AAAGCCACTC 900
CAGCTGACCT AGAGATCAAC AAGATGAAGC CAGTAGACCC ACAGATGACT GAGAAATGTG 960
TTTATTGCTG TATCTGTGCC ATGTCGATTT TTGTGGTTGT TTGCTGTATG TCACTATTTT 1020
GGCAATAGCT ATATATTCCC TTTTCCTTCT TCTCTGTGCT CTGGTCTGAA TTAATGCCTC 1080
TTTGTTTCAT CTCATTTCCC ATTGCTTTTC ACTTTATTAT 1120
|
