| Tag | Content |
|---|
EnhancerAtlas ID | HS010-02386 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr2:60640720-60641830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr2:60641317-60641332 | TGCCCACCCACGTTG | + | 6.51 | | RREB1 | MA0073.1 | chr2:60641035-60641055 | CCCCAAAACACAAGCCCTCC | + | 6.16 | | ZNF263 | MA0528.1 | chr2:60641271-60641292 | CCCTGCCCTTCCCCCTCCTCC | - | 6.1 | | ZNF263 | MA0528.1 | chr2:60641274-60641295 | TGCCCTTCCCCCTCCTCCTTT | - | 6.83 |
|
| | 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 |
| GH02I060412 | chr2 | 60639852 | 60641878 |
|
Enhancer Sequence | GAGTTTGCCT GTGCCATCTC ACAGATGGCA TGCTCCCTAA TCCTACAGCT TACTGCACGG 60
CTAGACACCA TCCGAGGGAC AGGGTAAGAC CGAGACAGCT CCTGCTCACC TCCCAGTTGG 120
CCCCACACCA TGCACACTCA GGTCCTGGTG AGGCCACTTG TCACCAGAAG GCCCATTATG 180
CTAACATGCA ACTAAGATAA AATGGATAAC TCTTAAGGGG GCAAAAGATC CCTCGTGGGA 240
AAGGCTCATG GTAAGAGAAC GCACCTCCCT GGAAACAGAT GTCTTGGTCC TATAACACAA 300
ATTGCAGTAT CACATCCCCA AAACACAAGC CCTCCCATAA ATCATTCAGG GGAGCCTGTT 360
TCGTTTTCCT GTTCTGATGA AAGTGACCTG CATGTGGGGC TCAAGGCCAA AAGCACTGCC 420
ACACTCGAGC AACTCCACAC TTCCCCACGG CTTACTGTAA AGATGCTGAC CAAAACCACC 480
AGGGCTGGAA CCGCTGCCCT GCCCAACCTG TAGAAGTTGG CATTCCCCAG GGTTCTGCCC 540
ACAGGCTGAG CCCCTGCCCT TCCCCCTCCT CCTTTGCCAA TCCTACCAAG TGCTCAATGC 600
CCACCCACGT TGGTCTCCTT TCTCCCACCT TTCTTGGATC ATCTCACACA GAGTTGGGGG 660
CTCCAGGTCC CATTTTTTAT CTTCTATAGT GCCCAGTCTA TGGCTCTGGT TTGGGCATTC 720
TCTCTGACTC TAACTTGCGT TGTTTGTTTC ACACAAACAT GTTCTCTCTC CACATTGTAT 780
TTTCTGTAGT CAACAAAAAT TCACCAACTG TAAGTGCGCA ATTGAATGAG TTTTGTCAAC 840
CATATACAAC CATATGACCA CCAGCACAGT GATGTGTAGA ACACTGACAT TATCTCTCAC 900
CTGTTTGCCA TCAATCCCCT ATCCAGGCCC CATGGCTGTT GGGAATCTCT GATGTGTCTT 960
CTATCACTAT TGTTTTGCCT TGTCTAGAGT TTTGCATTTT GCAATCATTC AGAATGTAGT 1020
CTTTGTGGTT GGCTTCTTTC ACATAGCATA TTCCTTGAGA TTCATCCACA TTGTTGCATG 1080
CATCTCAACA CATCATATGG TTGCATGCAT 1110
|
