| Tag | Content |
|---|
EnhancerAtlas ID | HS010-01928 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr17:47337110-47338340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:47337127-47337145 | GGGAAAAAGGCAGGAAGG | + | 6.31 | | FOSL1 | MA0477.1 | chr17:47338191-47338202 | CATGAGTCACC | - | 6.62 | | FOSL2 | MA0478.1 | chr17:47338192-47338203 | ATGAGTCACCC | - | 6.14 | | JUNB | MA0490.1 | chr17:47338192-47338203 | ATGAGTCACCC | - | 6.32 | | JUND | MA0491.1 | chr17:47338191-47338202 | CATGAGTCACC | - | 6.02 |
|
| | 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 |
| GH17I049259 | chr17 | 47336904 | 47338798 |
|
Enhancer Sequence | TGTGCACTGA GGGGTAGGGG AAAAAGGCAG GAAGGGGAGG GTGGAGTCAC CTCGCAAAAG 60
GAAGCCAGGG GAGCCCAGAA CAGGATCCAG GGTCTCCCTC CCCCGTGGTC TGGAGATCCT 120
TGACATCTGC CATCCCCTTA GCAGAAGCTG CAGCCAGAGA AAGAGGGCGA CGGTCCCGTC 180
ACATTCTGAG CCCAGCAACG GAGGGCTTTC CAGGCCGGGA CTGCGGGCAG ATGGGAATTC 240
TCCTCTCCTT TCTGCTGGAC GTATCTCCCC TCAGTTTCGC TATCTGTAAG ATGGGGCATT 300
GTCCCTGCCA AACCCGCAGG CCAGGACGGC CTAAGAGGAT CAAACGAGGA GAGGCAACGA 360
GGATTGGTGC CTGGCTTTTC CTGAAAACAG ATTCCTCCCC CGCCCCCGGG ACCTGTCCCA 420
CAGGGGCGTC TGGAAATTCC ACAGAGCCAG CCAGTCTCAG AGTGAAACAA TCGGATCCGC 480
CGCGACACAG CAGCTATTCA GACGTCGGGG GCGGGGGCCG GGCCGCTGAG CGAGCAGAGC 540
AATGCCGCCC TCGCGTCCCC TCCCGGCCCA CGCGGCTGCC CCGGCCGCCC TCCCCGCGGA 600
GCCCCGGCCT CGCACGGGCC TCGGCGCCCG CCGGGCGTCC CCCAAGCTTC CTTGTTTGTG 660
GCCGAGCGAC CGCGGAGCGT GGCACGTTCA GGAAGGACGA GTCGCCCCAC GGCGGGGAAC 720
CGGCGACCGG CGGCAGCCCC AGCCCAACCC CGGCCACGCC TCGTTAGGCG CCACGTCCCG 780
TCCCCGGGCG CCCGGAGCAC TGTGCCCCGC CGGCCCCTGC CCGCCGCTCG CTGTAGGAGG 840
GAGCCTTCTG CGTCGGCTCC CGACACTCGC TCACTGGGGC GCGGGCACTT GAGAGTAGGC 900
AACCTGGGGG CCCCAGAAGG GGATGGGGCT CCGACAGCTT CAGCCGGGCG TCCCCTCAGC 960
TGCCTTAGCT GGCGTCTGAG AGCGACTCCT CCGTCCAGGG CTGACAGTTC CCTTGCCCCT 1020
TAAGAGCCAA TCGGAGAATC ATAGGATCTG ACATCCTGTG GCTCAGCCGG GTCTAAGAGC 1080
TCATGAGTCA CCCTGTGTGC TTTGCTGATG AGGAAACCGA GGCCCAGAGA CGGGGGCTGA 1140
CTTATTCGAG CCACGTTTGT GTCTCCTAGC CCTGTGCCCT TTCTCCAACA CTCTACTATC 1200
CTACCTCAAA TCAAATCCAC TCTGGGGCTA 1230
|
