| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13666 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:99451790-99453130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr2:99452122-99452136 | GGGCCACGTCATTA | + | 6.01 | | FOSL1 | MA0477.1 | chr2:99452393-99452404 | GGTGACTCATC | + | 6.32 | | JUND | MA0491.1 | chr2:99452393-99452404 | GGTGACTCATC | + | 6.62 |
|
| | 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 |
| GH02I098835 | chr2 | 99451659 | 99453100 |
|
Enhancer Sequence | AGCCATTTCA CACCACAAGG AGGGAGCCAG GGTCCTGTCA AGAAAGTGCT GATTCCAGGT 60
CAGGGGAAGA AAATATACCA AATAAACCTG AGATTTCTCA TTGGACAAGA AAGTAAGGAA 120
GCCATCAAAG ATGAATGGGG TCATGTCAAA AGACGGAGCG AATTTCAAGT GACTCTCAAC 180
AGCCTAAGAT GGAACAACTT GAGCATTAAA ATGAATAAAG ACTGTCATGG ATTAAAGCAA 240
ATCAAATATA TAAAAAGTAA TGCATTCCCA ATGATATTTG GAAAAAAAAA GAAAAAAACA 300
AAACCCACTG GCCACTGTCA GGAGTTGCTA GGGGGCCACG TCATTACTCT GAGGGTGGAT 360
CAATAAAAGG AGAGCCAAGC ATGATCCTGA CTTTACAAAT TGTATTTCGG AGCAACCAAG 420
CAATTGATGA AGGAAAGTTC TTCATCAAAG AATTTCAGTT AGCAAGTGTA CAGTGAATGA 480
TAGAATTAGA AAAACCACCA CTTTGTGACA AAATAACAGA TCATCACCAG GTGTTAAAAC 540
TGTCAGGTGA AGGTTGGTGG AGGGACGACA GTGACACACC CTGAACCCAC TGCTCAGAAA 600
GCAGGTGACT CATCATGGGA TGTGACAACA ACCAGCACCT GCTTGAACCT GACAGAATCT 660
GGATCCATCG AATGATGTAC CGGGAATTGG GAGAATATAG GAAAGAGTTG AGTCACACCA 720
AGAGAAAGCA AAGCCAGAAT ATGGGACATT CTGCAGGACA CATGGCCCTG CTCTTCCTTC 780
AGATCAATGA CGTGAAACAA AGGGAGAGGG CAAAAGGAAA TCGTTATAGA TTAACAGACT 840
TAAGAAGCAC AACCGCACAG ACACAGACAC GATAAATGGG CGTCACTTTA TTCAACCCAC 900
AGGGTCCCAT GTGGTTTGCT CGCACTAATG TGCCTTAGTA AATGGAGCTG TTTTCCCCAC 960
AGTGATGGAT GAGAAGTTGC CGCAGACTCT CCCACAGGCC AAGCAGTACT TGCCTCTTCC 1020
TCTGTGCTGC TCTCTAAAAA TGTCATTTGC ACTTCCCAGG CCTCATCATG CTCCATTCCC 1080
AATCTTCCTT GCCTAGCATC AAAACCAGCA AACTGTTACC AGTCACTGAG GGCCAGCTCC 1140
CTGCAAGGTG CTGGGAATAT CAAGATAAAA AGCACACCGT CTCCACTTTC CATGGGCTCC 1200
TGTGACAGGG AGGACATCAG CAAGCGGACA GGACAATTCA TCCCAGCTTG CCCCTCTGGC 1260
TGGGCTCCTG TCTGTGGTTG GAGGGGCCAC TCCCAGGCCT GTCTCTCCAA CACCAGAACT 1320
GTGTGCTCCA GTCAAGAGAC 1340
|
