| Tag | Content |
|---|
EnhancerAtlas ID | HS060-19245 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:60640140-60641690 |
SNPs | | Number: 2 | 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 | TAATAATAAT AATAAGGGGT AGCTAGTACT AACCCTCCCT CCCCAATCAA ACTCCGCATG 60
GGGCTTTCTT CCTCTACCTG TCTGACAGGG GAAAGTGGGC AGGGGCAAAC CTCCTCCCAA 120
ATTCCCCTTC TGAGAAGGGG TAGGAGGTGG GGTGCTTGTC CGTCACAGGT ACACATTGTG 180
TTTCCATCTA CATGCACCAT GCCATGCCCC CACTGCTTGT AGACAAAAAG GAATGAGTCA 240
AATAACTGTC AAGTGACTCA ACACTTGACA GGCTGTGTGG CCATTATGTG GGTCCCTTCC 300
ATACTGGCTC CTGGTGACTG AAGCCAGCCT CAGTTTTGTC CTCTGTGATG TGAGGACTTG 360
AGCAAGAACC TTGCCAAAGC TCCCCTAGCC AGGATACTCT ACAATTGCAC ACCCCTGGCT 420
TCAGGCCTCC CCAGGGAACT TTACCTCCTG GTGAGAAGGG GTTGTGGGCC AAGATCTGCT 480
GGCAGCAGAG CTCCCCAGCA TGGGCCATTA ATCCACATGG GGACAGTTAG CATAACTGAA 540
ATTTAATCAA ATAAATGGCT AAAACTTAAT TGTTAAGTGG GAGTTTGCCT GTGCCATCTC 600
ACAGATGGCA TGCTCCCTAA TCCTACAGCT TACTGCACGG CTAGACACCA TCCGAGGGAC 660
AGGGTAAGAC CGAGACAGCT CCTGCTCACC TCCCAGTTGG CCCCACACCA TGCACACTCA 720
GGTCCTGGTG AGGCCACTTG TCACCAGAAG GCCCATTATG CTAACATGCA ACTAAGATAA 780
AATGGATAAC TCTTAAGGGG GCAAAAGATC CCTCGTGGGA AAGGCTCATG GTAAGAGAAC 840
GCACCTCCCT GGAAACAGAT GTCTTGGTCC TATAACACAA ATTGCAGTAT CACATCCCCA 900
AAACACAAGC CCTCCCATAA ATCATTCAGG GGAGCCTGTT TCGTTTTCCT GTTCTGATGA 960
AAGTGACCTG CATGTGGGGC TCAAGGCCAA AAGCACTGCC ACACTCGAGC AACTCCACAC 1020
TTCCCCACGG CTTACTGTAA AGATGCTGAC CAAAACCACC AGGGCTGGAA CCGCTGCCCT 1080
GCCCAACCTG TAGAAGTTGG CATTCCCCAG GGTTCTGCCC ACAGGCTGAG CCCCTGCCCT 1140
TCCCCCTCCT CCTTTGCCAA TCCTACCAAG TGCTCAATGC CCACCCACGT TGGTCTCCTT 1200
TCTCCCACCT TTCTTGGATC ATCTCACACA GAGTTGGGGG CTCCAGGTCC CATTTTTTAT 1260
CTTCTATAGT GCCCAGTCTA TGGCTCTGGT TTGGGCATTC TCTCTGACTC TAACTTGCGT 1320
TGTTTGTTTC ACACAAACAT GTTCTCTCTC CACATTGTAT TTTCTGTAGT CAACAAAAAT 1380
TCACCAACTG TAAGTGCGCA ATTGAATGAG TTTTGTCAAC CATATACAAC CATATGACCA 1440
CCAGCACAGT GATGTGTAGA ACACTGACAT TATCTCTCAC CTGTTTGCCA TCAATCCCCT 1500
ATCCAGGCCC CATGGCTGTT GGGAATCTCT GATGTGTCTT CTATCACTAT 1550
|
