| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17686 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:45128750-45130060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr19:45129741-45129752 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr19:45129741-45129752 | GACAGCTGCAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_37773 | chr19:45125498-45131554 | HSMMtube | | SE_38302 | chr19:45128157-45130715 | HUVEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 45129392 | 45129792 | | chr19 | 45129025 | 45129914 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I044624 | chr19 | 45128222 | 45131202 |
|
Enhancer Sequence | GTCAAAACTC AGTTCAGTCC CTGTTCCCGT GCCTTCCTGG CTGGGTAACT TAGCGCAAGT 60
GACTTCCCCT CTCTGAGCCC CAGTTTCCTC ATGTGTATAA TGGAGGTAAT CCTATATACC 120
TCTTCAGGGT TGTTATAAGG AACGAAAACA AGGGGTGACT GAGTTTGGCA GAACAACTGT 180
CAGGCAGCAG GTGCCTTGAA TAGCAGCTGT TATGGTGAAT ATTGTTTTTA GTGTGTTATT 240
CATGGAGGGA CACATGGTGA TATGGTTTGG CTGTGTCCCC ACCCAAATCT CATCCTGAAT 300
TGTAGCTCTC ATAATCCCCA TGTGTCATGA GAGGGACCCG GTAGGAGGTA ACTGAATCAT 360
GGGGTCAAGT TTTTCCCATG CTGTTCTCGT GATAGTCAAT AAGTCTCACG AGTTCTGATG 420
GTTTTACAAA AGGCAGTTCC CCTGCACACA TTCTCTTGCC TGCCGCCATG TAAGACATGC 480
CTTGCTCCTC CTTCACCTTC TGCCATGATT GTGAGGCCTC CCCAGCCATG TGGAACTGGG 540
AGTCCATTAA ACCTCCTTTT TTTTAATAAA GTACCCAGTC TCAGGTATTT CTTCATAGCA 600
GTATGAAAAT GGACTACCAT GGCTTGGAGT GAACTAGAGG TATGCAGAGG AACTGGCCAG 660
GAGAGAAGAG AGGGAGGGTA TTTGGGGTAG GAAAGAATGC ATGAGTCAAG GTTCAGAGCT 720
GGGACATGGA AATGGAATGC GTGATGGGAA TCTCAGCTTG GCTGGGTCCC AGAGAACCAC 780
CTCACCTCCC TGGCCAGGGT CCAGTGGGAG CTTCAGGGCT GATGCACTGG GGGAAAAAAT 840
GTAAATCTTA TATCACCTAG TGACCCTGAT ATTCAGTGAG AAGGACAATA CTTCCAAGAC 900
CTCCTTTGCT CATTCATCAA CTGCCCAGGA AATGTTTATG AGCACTTGCT GTGTGGCCAG 960
CCCACACAGC TGGGAACACT CTGGTGACCA AGACAGCTGC AGCCCTGCCT TCACAAGACT 1020
TACAGTCCAG TGTCCACAGA CAGTGATCAC CAGAGTGGGC AGGGCTGGGA TGGGGGAGCC 1080
CAGAGAGCTA TGAGACTCAG CCTAGGAGTT AAGGAGGGCT TCCTGGAAGA AGGGACACCT 1140
GAGCTGAGAA TTATGCTTAG CTGGCCAGGT ACAGTGGCTC ATTCCTGTAA TCTCAGCACT 1200
TTGGGAGGTT GAGGCGGGTG GGTCACTTGA GGCTAGGAGT TTGAGACCAC GCTGGCCAAC 1260
ATGGTGAAGT AGATGGTGAA GAAGATGGTG AAACCCCATC TCTACTAAAA 1310
|
