| Tag | Content |
|---|
EnhancerAtlas ID | HS047-28941 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:36816090-36817270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr6:36816404-36816414 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr6:36816404-36816414 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr6:36816404-36816414 | AATGGAAAAT | - | 6.02 | | ZNF263 | MA0528.1 | chr6:36816546-36816567 | CTCTCCTTTCTCTCCTGCTCC | - | 7.2 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_30666 | chr6:36816035-36817429 | Fetal_Muscle | | SE_41488 | chr6:36815093-36821882 | Left_Ventricle | | SE_48751 | chr6:36814793-36817300 | Right_Atrium |
|
| | 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 |
| GH06I036848 | chr6 | 36816041 | 36817376 |
|
Enhancer Sequence | AGCCTGGATT CTCGCAGTCT AACCGAGTTT CTTTTTCCAC TGAACACCCA AGCTCTTCAC 60
TTTGGTGGAT GTTTCCCCTT TCTCCCTTGG CAGGGGATGT GTCCTGATGG CAGGGACTGG 120
GCCTTCTTAC CCTGGTCCTC CACAGCCTGG CCTTTCCCAG CCTCAGCCTC AGCCTCCTTC 180
TCTTTCTTTG TGCTGGGTTT AATTTCATTT AAGTACATTA CCCGCCAAGC CAGCCAGTCT 240
ACTCGTAGGC CTCCTGAACT CTCTCTCTGT CCATTCAATG TAAACCCATT TCCTCTTGTT 300
TCAGCATCTT GGGAAATGGA AAATGAGTCC TCACATTTCT TCGGATGCTT AAAAGCAAAC 360
TAGGTCCCAC CCTGAAGTCT CAGCCTCCCA ACACTTGATG CCTTCCTGAT TGGCATCAAG 420
GGCGGAGACG GAGCAGCTGA TTTTCACGTG GGCGGCCTCT CCTTTCTCTC CTGCTCCAGC 480
GGCTGTGAGG GTTATCGGCT CAAGCTGCAG GACTCCGCCC CTCCCTCCCT CAGGCCATGT 540
GTGTGGGAGG GGAAGGGAAC TGACATTTCA CTCCAGCCCT TAGATTCTTT GTCACCACTG 600
CTCCTTGGCA CCTGCCTCCC CTGGCTGTAC CTGTACCGGG GCAGCCTGAG AAGCCACCGA 660
GGGTGAAACA CTTCTTTTCT TTTAAGCTCT AAATTCATTT TCATGCCAAG CTGCTTGTAT 720
TTGCCTGCCT GGCTGCCGAA GGTAACTGAA ATGTGCACAA AATGCCACAA GCCTGGCTTT 780
GTGCGGAAGC TTAAGTCCCG GTGGCCCTGC CCCCAGGGCT CGCCTGCTCG CTCGCATCTC 840
CAGCAGCCCG CCGAGATTTC CTTGGGTTTT ATTAGCTCTG ACCCTACACT GGGAGAGGAA 900
CTCATCAGAC ACACTTCACA TCTTGCCTCC TCCACCTCTG GCTAAGAACC GTCGCCCCGA 960
TTACGGGAAG TATTTGTTCC CCAGTTCTCT GATAATTCTG TCAGGAGCCT GCGTAAGGCT 1020
CAAGTGTCAG GCTGCAGGAG CTGCTGCTGA CAGCCCCTTG GAGGCAGCTG GCCTGCGGAG 1080
GGGGCCGGCG GGGGAGTTTG CAACAGAGTG CCGGGTTCTC TGGTCTCTTC CTCCAGCTTA 1140
AAAATGGGGT TAATAATATA ACCATACTAC CATTCCTTCC 1180
|
