| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13713 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:102622500-102623680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:102622879-102622898 | TCACCAGAAGGGGGAGCTC | + | 6.05 | | ELK4 | MA0076.2 | chr2:102623251-102623262 | CCACTTCCGGC | + | 6.62 | | Gabpa | MA0062.2 | chr2:102623250-102623261 | CCCACTTCCGG | - | 6.02 | | TEAD1 | MA0090.2 | chr2:102623302-102623312 | ATGGAATGTG | - | 6.02 | | ZBTB7A | MA0750.2 | chr2:102623250-102623263 | CCCACTTCCGGCC | - | 6.87 |
|
| | 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 |
| GH02I102006 | chr2 | 102622801 | 102622970 |
|
Enhancer Sequence | TATTTGGCAC AATAGCTATT GTTATACACT AGTCCCTAAA ACACCAGCTT TGACTTCATT 60
TACTTATCCT GATATATGGT ATTGGTTAGC TACAGTGTAT TTAAATTCCT ACTTCTTTCA 120
TGTTCTAATG GTGCACTAAT GAGTCTGGCT TGGACCAGTA TAGTTGGGGA TGTGATAAGC 180
TAATGCGTGT CCAAGGAGGA CACAGCAGCT TGGTGGATGT TTATGTGACC TTCATCTGGC 240
AAACCTGACA GTATGGTTAG GGGTAAAGTC ACAGGAACTA TTTGTGCTTC AGAAACTCGT 300
GAAGAATAGT ATTGTGTAGA AACAGAGTTT AAGGGAGAAA GCTCCAGGCT AGATACATAG 360
CTAAGGGGAA TATCTCAGGT CACCAGAAGG GGGAGCTCAG ACTGTAACTC TGAGTCCTTG 420
GACTCAGGGT TCCCCACTCA CGAGGGAGGG TTTCTGGAGT GCGAGGGTCG GTTCCTCAAT 480
GCCGCAATGC CGCCCTGGAT TTACTGCAAG TCATTCCCAG AGATATCTGT GCAAGGAGCA 540
GGGAACAACT CAAGGTAAAA GTGGCTGGGA ATTTTTCCCC TGGATTCATT CACAACTCCT 600
GCCGTGGGCA GGCTTTTAGT CATAAGTATT CCCCGGTATG TTCTAGTGTG TGGGCCATGA 660
GGGCTGTGAG CAAGACCAGG GCTCTGCCCC AAGGTTGTCA CCATCCTTGC GGAGCCAGAA 720
GAGTCAGGCA TGGCAGCTGG CACGACTGCT CCCACTTCCG GCCCTGCCGA TGGCCGGGTG 780
GGGCATTGAC TTGCTGTGTC GGATGGAATG TGAGCAGACA AGAGTGAGTT AGTTCCCAGT 840
GTGGCCTCGT GTGTGCTTTT GGCCGCATCG TTTCCAGTTT CGCCATCCCC AAAGAGGATC 900
ATCTCCCAGG AAGCTTACTG GTCCAAGGAG GATGAGACAC CCATGGAGCA GACTTGGACC 960
CCATCTGCCG CTCAGAGCCA GGCCTAACCC TGCCAAGTTT AGGTTAACCA ACTTCCATCT 1020
TGCCCACAGA CTTGTGAGCA AGAGTGAACG ACCGTTGTTT CACACCATTC AGTTCTGGGG 1080
TCGTTGGTTT GTTAAGCAGC ATCGTTGTGG CCGTGGTTAG CAGACACAGG GAACACTTGT 1140
GATAGTGTGA GAAGGTCATC AGGGAGACGA GGAGGGCATC 1180
|
