| Tag | Content |
|---|
EnhancerAtlas ID | HS187-02697 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr10:1155760-1157160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr10:1156298-1156312 | AGGAAATGAGTCAT | + | 7.28 | | Six3 | MA0631.1 | chr10:1157006-1157023 | TTTAGTGATACCCCTTA | - | 6.09 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 1155793 | 1156694 | | chr10 | 1156816 | 1156952 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I001109 | chr10 | 1155641 | 1157181 |
|
Enhancer Sequence | AGTGTTATGA AAAAGTTCTT ACTAATGTGG ACCTATGAAT ACAGTTTCCT AGGGTTTATG 60
TCTTCCTATT GGAATCAGGT GTGGGGGTAG AGTAAGGTGG AGTGTGTAAT TCCCGTGTGC 120
CCTTTCTCCC ACATGGGTCT TCCAGGCTGT AGGCTGTGCT TCCATTCACC TGAACCACGG 180
GGGTGAGGTG AACGTGGACC AGACCTGCCC GGGCCATGCT TACTCAGATC GTTTACGCTT 240
TCTTTTTTCT TACTCAAATT ATCATGAACT AGCGTATCTT GTTGATGTGT ACATCCAAAA 300
ATACGTTTTG AAAAGATCTC TCTTTGGCGC TAATTTTGTT GCTGTGTCGG GGCGAGTCCG 360
CTGGGCTGTT GGACATTGAG CTTCCCCTCA CCGGCCTGGC GGTTTCTCAG CTGTGCGCAT 420
GCAGGATGAG GGCTTGGTCA GCAGGTGGAG CCGTGGACGC CTTTATTGAA CACAAACTCT 480
TCCTTCCTGA CATCAGATCA GCTGTAAACC TTTAGACGTG CCTCATAATG AGAAAAGCAG 540
GAAATGAGTC ATTTTACAAA AATGTTTCAT CTGAGGTGTC TTCTTAGTAA CACTTGCCTT 600
TGTCTCCGGC ATGGGTTTTG TAGGTTCGAG CCAATACGAC AAATAAAACC TACAGAGTGC 660
GTGATCCTTA CAAATGTGTA GAGCTGTGCA TCCGCGCCAC AGCACACCAG GGTGAGGGCC 720
TCGCAGTGCG GTTTAGGTCC TGAGATGTGC GTCCGCGCCC CAGCACACCT GGGTGAGGTC 780
CGGGGTGCGG GTTTAGTTCC TGAGAGGAAT GGCCAGGTTG TGTGTGTGTG TTCCGTTTGG 840
TCACTTGTCT GGGACGTTCT GAACATGACT TGTAAGAGCA CACCCTGGGT CCCCTGCCTT 900
CCCTGCCACC ATGTCATTCT GAGGGACCCT CTGCGCCGGG GGCTTCTCTG CAGTGGCCAC 960
GGCATCGCCA AGGACATCCG TGAGCCTCCG ATGGGTGTCC AGCGTGTTAG CGCCCAGACC 1020
CACAGGGCCT GGCACCCTGA TAGGTGGGAA TGTTGGCCCA GGGCCGGGCC TGAGGCCTGC 1080
AGGACTGCCT GCTCATCCGG GAAGTAGCTC TGCCGGTTTT ACAGGGTGAT CCTGAGTTCT 1140
TTTCACTAGT TCTTTTCCTG AGCATTGAAA GCAAAAGTCA GACATGTGTT CTTAGGAAGT 1200
TTGCTGTTCT TGTTGATGTA GGCTGGAAAG TTATATGCAT GGTGTTTTTA GTGATACCCC 1260
TTAAACAGAG GCAGTATTTC TTCAACATGT GTGACTAAAA ATACCCTTTC TCACATAATT 1320
TATATTAACA TGATGTGGAA TGTGCTTTTC AAAGTTTTAT CTTAGGGCGT ATTTTCACTT 1380
GTAGGAACTA AGCGTAAATT 1400
|
