| Tag | Content |
|---|
EnhancerAtlas ID | HS191-08563 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr12:13144870-13146020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:13145885-13145906 | ATGGTGAAACTGAAACAAAAA | - | 6.81 | | Nfe2l2 | MA0150.2 | chr12:13145562-13145577 | TGCTGAATCATTCTG | - | 6.78 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_46589 | chr12:13143937-13147247 | Osteoblasts |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 13145446 | 13145954 | | chr12 | 13145478 | 13145960 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I012990 | chr12 | 13143372 | 13147333 |
|
Enhancer Sequence | TATACCACAG AGCTTTACAT GTGAGAAGTG CAACAGATAT TTATTTGATT AAGGTGCTGT 60
GTCTCCTAAC AATGATTATG AAAAACAGAC ACATGGTAGG GAACCTGGCT GCCCTAGACT 120
GGTCAAATAG GTTTTCATAT AATATCCTAG ACTGAAGATT CACAACTAGG GAAGAGGGTG 180
TGACTCCCAG GGGGACAGAA GGTGTCTCTG GAGGAAGGCA GGACTGTACG GCTGTGAGTG 240
GCAAGTGTAG TCTCAATGAG CATATTTAAT ATTTATTTTA TTTTTGAGAC AGAGTCTTGC 300
TCTGTCACCC GGGCTGGAGT GCAGTGGTGT GATCTCTGCT AAGAGCAACC TTCACCCCCC 360
AGGTTCAAGT GATTCTTCTG CCTCAGCCTC ACAAGTAGCT GAGACTACAG GCGAACGCCA 420
CCACTCCCAG CTAATTTTTG TGTTTTTAGT AGAGATGGGG TTTTGCCACA TTGGACAGAC 480
TGGTCTCGAA CTCCTGACCT CAGGTGTTCT GCCCACCTCG GCCTCCCAAA GTGCTGGGAT 540
TACAGGTATG AGCCACTGTG CCCGGCCTTA ATATTGTAAT TTTAACCCTG AGTGCCAAGT 600
TTGTACTTAA ATCCCCCTTC ACATGGGGTA GAGGAAATTG CGCCAGACCA GGAATCATGA 660
GGCAGCAAGT CAGCCTTGAC TGTGGGGCAC CGTGCTGAAT CATTCTGAGG CTGCTGTGAA 720
GCCCTCCATC TGGTGAATCT GACACTTCCA AAGAGCCTTC AGTAGCAAAC TGTTAAGTAA 780
ACTTAGGGTG TTTTGCTCTT TCTGTTGCTG CAGAGAATTC CAGAACTCCC CTTTCATTTG 840
AGAGCGCACC TACCCTTGGC ACTTGTAATG TTTTAAATTC CAGAAACACT ATCCTGTGAA 900
TCACAGAAGT TCAGAACCTA AAATGGTTTT AAAGTTTACC TAATCTAACT AATTTTATCA 960
AGGAGAAAAT GAAGAACCAG AGAGACTAAG TTGCTCAAAG TGATGTAACT ACTGAATGGT 1020
GAAACTGAAA CAAAAATTCC AGTTCCCAAA CTCTAGTCTA CTCCAGTCTA ATACTCGTTG 1080
CAAGGTTCTC TAAAGCTATG GGGGGTGAAG TGAGCATTTA AACCTCTGTT TCTTTTCTTT 1140
ATCCTCCTTT 1150
|
