| Tag | Content |
|---|
EnhancerAtlas ID | HS056-16130 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chrX:22010830-22012000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chrX:22011969-22011987 | CCCTCCTTCCTTCCCTCT | - | 6.84 | | EWSR1-FLI1 | MA0149.1 | chrX:22011965-22011983 | CTCTCCCTCCTTCCTTCC | - | 7.37 | | Foxq1 | MA0040.1 | chrX:22010912-22010923 | AATAAACAATT | - | 6.02 | | MYB | MA0100.3 | chrX:22011839-22011849 | ACCAACTGTC | + | 6.02 | | ZNF263 | MA0528.1 | chrX:22011961-22011982 | TTCTCTCTCCCTCCTTCCTTC | - | 6.67 | | ZNF263 | MA0528.1 | chrX:22011979-22012000 | TTCCCTCTCCTTTCCTCCTCT | - | 6.78 | | ZNF263 | MA0528.1 | chrX:22011976-22011997 | TCCTTCCCTCTCCTTTCCTCC | - | 6 |
|
| | 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 |
| GH0XI021992 | chrX | 22010719 | 22012518 |
|
Enhancer Sequence | GTATCCTTTG ACCGTGACAT TCTGTTGCCA GATCAAAGCA CCCAAGTAAA TCATATGCCA 60
ATGAAAAAAT TTAAATCACA ATAATAAACA ATTAGCTTAG CCATAGAGTA TATAAAGCCC 120
TGGTTCTCCA GCTTAGGTGC ACATTGGAAT CCCCTGAGAA GCTTTAAATA AAATCTGAGA 180
TTCTAGACTT CCATTCTCAA AAGTTTTGGG GTCTGGCTTG CCACAGCTTT CCAGGTGCTT 240
TTAATGATCA AGCACTACTG GTCTAAAGCA TTGGTTCTCA AAGGTGTTGC CAGACCTGCA 300
GCATCGCTCA AGAACTAGTT AGACATGGAC ATTCTCAAGC CCCACCCCAA CCTGCTGCCC 360
AATCAGAGGA ATTCTGGAGG TGGGGGCCCA GTGACCTGTT CTACCAGCCC TCCCAGGGAT 420
TTATGTGCAC CTGAAAAGTT TGAGAAGCCC TAGTCTAAAA TAACCACCCT ACCTGTGGCA 480
GGTAAAATGT CTAAAGACAC TCATTCTACT CTTACATTAA AATAACCTGA CATTAATACT 540
AGTTTCTACA CTTGATGCTA ATTTGCAACA GAAATCGAGA ACTAGAATGA TGTTGGGGAC 600
TGCACGGTTA ACATTGGTGT TCTCTGTTAG TTCCGCTTAG TAAAGTTAGT CTAGAGAAGT 660
AAAACACAGA AAGAAAAAAG GAAATGAGCA TTATCATTGG AAATTTGTGC CGCAACACAG 720
CTGTGGGCTG TAGTCTGCAG ATGACGGCTT CCTTATCTGC TGTTGCCAAG TCCAGGTTCC 780
TGTGACGGCA GGGTTTTTTT GCTGTCAAGG GAGCAACTGC TGCTGACCTC CAGTGAGGCC 840
TGGTCCCATC AGGCTGGGGC AGAGCCCGAC GGGGCAAACT GCCTGCTGAG ACCAGATGGC 900
CAGCAAGAGG CAATGAGAAC CCTCTAGATC CTCCATGTGA GGAGGGGAGT ACTCCGCCTG 960
CTGGGTGGCC GTGTCCCTCC ACAGCCTGTA CAGAGCTTCA GCATCTCCTA CCAACTGTCC 1020
ACCTTTGTTT AGGGTTCCCC TCAGCATTTT TGTCAGGCCT GTGTTTGCAT GTTGGGAGAT 1080
TTGAGAAATC AGTTGATAAC ATTTGAGGCA AAGTCTTCCA CCTGCTAGTT CTTCTCTCTC 1140
CCTCCTTCCT TCCCTCTCCT TTCCTCCTCT 1170
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