| Tag | Content |
|---|
EnhancerAtlas ID | HS010-00767 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr11:9385540-9386460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr11:9385932-9385947 | CGCTGAGTCATGGTG | - | 6.43 | | TCF7L2 | MA0523.1 | chr11:9386372-9386386 | GAAGATCAAAGGCA | + | 7.31 |
|
| | 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 |
| GH11I009361 | chr11 | 9382592 | 9387533 |
|
Enhancer Sequence | GGGGGTAGGA GTGGGGGTAG GAGTAGGGGA GTGTCACACA TCTGCAAACG GTAACGTTGA 60
ACTTCCAAAG TAGGTCCATC GGGCTCTCAG GACCCGCGGC TGTCCGAGGC CTCAGTTGCC 120
TCAATTAGTC TTAGGCTAAC TTCCTCCTTG CGCTGGGGGG TGGGGAATAC TTTCCCGTGC 180
GGAGGCCTCA GCTCCTCAAT GTACAGAGAA GAGCCTTGCA GGGCCTAAAC ACTGGAGTTC 240
AGGGATCCTT TATCAAGCTG CCAAACCTTT TCAGGGGCTT GGAAGGACAC CTAAGGGCGG 300
AAGCGGGCGC GTTGTGGCCC CCGTGGGGCA GTGGGAAGGC AGCAGGGCCT CGCGGGCGGA 360
GGCCGGAGCG CCGCTGACGC CGGAGCGGAA GCCGCTGAGT CATGGTGGGG GCAGGAATGC 420
AGCGCATTTG GAGAAGGCCC GGGACGCCGG CGGCTCCAGC ATTACTGAGC AGTGACTTGG 480
CGTCCGCACC TTCACTGCAG TCGGGAACCA CCAGTGACGG CGGTGACCGG AAGAGCTGAG 540
TCACCGCAGG CGACGGCGAG CGACGCCGGC GGGGAGGGGC TGACGCGCCT GGGGCCGCGC 600
GCCTGGGCTC CAGGGCCCCG CGCGTCGCCA CGATCCCGAC GTTGCAATCC CCGCCAGCTC 660
GGCGGGGGCC GCACGGGGCT GGGTCTCCCG GATCCCGCCC GGGGATTGGA GTCTGAGGCT 720
GAAATTTGAA ATCTTGAAGT GGCCCCAAGC CACAAATACT ACAGACTGGT TTCAGTGGGA 780
ATTAGGACCT TGTGAAAGGA GACAGCAGTG CCCCAAAGAC TGGGTAGATT TTGAAGATCA 840
AAGGCACTTG CCTAGGAACA AAAATGATTT GCCTGACTCA GTTCCAAAAT GCAGCAAATA 900
ATAATTAAAG CGAAACACAC 920
|
