| Tag | Content |
|---|
EnhancerAtlas ID | HS010-00595 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr10:44090270-44091730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr10:44091182-44091200 | CTTTCCTTCCATTCCTCC | - | 6.25 | | IRF1 | MA0050.2 | chr10:44090835-44090856 | TCTTACTTTCATTTTTGGCTC | + | 6.36 |
|
| | 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 |
| GH10I043594 | chr10 | 44090109 | 44092350 |
|
Enhancer Sequence | TGCATGGGCT TCAAGCTGGT GGAGAGCTGC CTGGGTTACT CTCCTGTGTT CCTCAGTGTT 60
AAACAGTGTG AGAAGAAGCT GCCTGCAGTT TGGCCAGGTT AGATTGTGTG TCAGAAGGAT 120
GGACTGCATC AGATCTATAA GAGCTTGGGG ATTCTCCATA TAGGAGGGAG TATGGTGTTT 180
CCAGTTTAAG AGATCAGTGG TTGAAAAGGG CTGATAGATG CAAGTCCGTT GCCCCCCCTG 240
GACTTGGCCT TGGTCATCAC AATAAATGGG TCCTCACGTC TCCCTGAGAG GCACTTGCAT 300
AGCTTAAGCA TGGTCAGATC TGAGACGGCC TGCTTGACTA TCTTGACTTC CTTCCCTGGC 360
CTCTCGAGGC TCCGATCCTT CCCTTTGGGG TGAAACCTGG GGTGTGCTAG CTCCTGAATT 420
TCGTTCTTGG GGGGCTGTTG GCCTCAGCAA AGGGTGGAAC ACATGGAGGA AGAATCTCTG 480
CTCCTTCTGG CAGCTCCTGC AAGACTGGCT TCTTTTGCTT CCTCTGGGAC TTTCCCTTTA 540
ACTCTGTGTC TGCCAGCGAA GCTGCTCTTA CTTTCATTTT TGGCTCAGCT CAGGCCACAA 600
GTGTTTTCTG ATAAGCTGCT AAACAGGGCT GGATCCAGGC CAGTCTTGTT TGTACTATAT 660
TTAACCATGA GTCAATATAA GAAATTGATC TGGATGCCCA GGCTGTCCTC CGACCCCTGT 720
CACCACCTTA AATACATGGC CAATTATTTC CCTGTCTATA GTTCCTTTGG TCAGCCATCC 780
AATACCAAAA GGAGGCCATT CTAATTCACA GAGAGTTCTC AACCTTTGGG GGGTCAGCTT 840
AACTCCATAA TCCCCTGCAA AATATTTCTT AAAGGTCTGT AACTTGCACT CCAATGGAGT 900
GGGTTTTGAT GACTTTCCTT CCATTCCTCC CTTTGTGGCG CAGTACACTC ACTGTTCCTT 960
TTGCCTCAGG CTGACCAGAC TGTCTCCTAT TGAGGGAGTT TTCAGATGCC GCTTAGCTTT 1020
GGAGGGGTTC TTATTCCCAC CACAACTCTG AGCTGTGGGG CAGCTCCTAT TAGTTGCATG 1080
CAGCTTGCCA CTAGTCCAGG TCAGCCCCAC ACTTTGCTTG GAGCACACAG TGCACGCTAA 1140
GAGATTTATG ACTCCCCACA TCACTCCCCG CATTGGTTCC TTTTGAAACT GTTTCTTTCA 1200
CACACTTTCA CACACCTCCC CACTCCCAGT TCCTGTGTTC CTATTTAGGG TAGTGAGCCA 1260
CTCTCACCAC CTCCAATTTC CTTTTCCTAA CCAACTTAGT GAGCCACTCT CGCATCCTGT 1320
GTTGGTTGGG GTGTGAGTTT AATCTAAATT GGTGAGCCAC TCTCACTGCT CCCTACCTCT 1380
CTGGGTCGGA TTATGAGTTA CACCCCAGGA GGTGATCAGG CTCCCCTTCT GTCCTTATGG 1440
AACAGGTCCT GCCTTGGGCC 1460
|
