| Tag | Content |
|---|
EnhancerAtlas ID | HS034-15399 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:45128740-45130020 |
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 | TTGGGACCTG GTCAAAACTC AGTTCAGTCC CTGTTCCCGT GCCTTCCTGG CTGGGTAACT 60
TAGCGCAAGT GACTTCCCCT CTCTGAGCCC CAGTTTCCTC ATGTGTATAA TGGAGGTAAT 120
CCTATATACC TCTTCAGGGT TGTTATAAGG AACGAAAACA AGGGGTGACT GAGTTTGGCA 180
GAACAACTGT CAGGCAGCAG GTGCCTTGAA TAGCAGCTGT TATGGTGAAT ATTGTTTTTA 240
GTGTGTTATT CATGGAGGGA CACATGGTGA TATGGTTTGG CTGTGTCCCC ACCCAAATCT 300
CATCCTGAAT TGTAGCTCTC ATAATCCCCA TGTGTCATGA GAGGGACCCG GTAGGAGGTA 360
ACTGAATCAT GGGGTCAAGT TTTTCCCATG CTGTTCTCGT GATAGTCAAT AAGTCTCACG 420
AGTTCTGATG GTTTTACAAA AGGCAGTTCC CCTGCACACA TTCTCTTGCC TGCCGCCATG 480
TAAGACATGC CTTGCTCCTC CTTCACCTTC TGCCATGATT GTGAGGCCTC CCCAGCCATG 540
TGGAACTGGG AGTCCATTAA ACCTCCTTTT TTTTAATAAA GTACCCAGTC TCAGGTATTT 600
CTTCATAGCA GTATGAAAAT GGACTACCAT GGCTTGGAGT GAACTAGAGG TATGCAGAGG 660
AACTGGCCAG GAGAGAAGAG AGGGAGGGTA TTTGGGGTAG GAAAGAATGC ATGAGTCAAG 720
GTTCAGAGCT GGGACATGGA AATGGAATGC GTGATGGGAA TCTCAGCTTG GCTGGGTCCC 780
AGAGAACCAC CTCACCTCCC TGGCCAGGGT CCAGTGGGAG CTTCAGGGCT GATGCACTGG 840
GGGAAAAAAT GTAAATCTTA TATCACCTAG TGACCCTGAT ATTCAGTGAG AAGGACAATA 900
CTTCCAAGAC CTCCTTTGCT CATTCATCAA CTGCCCAGGA AATGTTTATG AGCACTTGCT 960
GTGTGGCCAG CCCACACAGC TGGGAACACT CTGGTGACCA AGACAGCTGC AGCCCTGCCT 1020
TCACAAGACT TACAGTCCAG TGTCCACAGA CAGTGATCAC CAGAGTGGGC AGGGCTGGGA 1080
TGGGGGAGCC CAGAGAGCTA TGAGACTCAG CCTAGGAGTT AAGGAGGGCT TCCTGGAAGA 1140
AGGGACACCT GAGCTGAGAA TTATGCTTAG CTGGCCAGGT ACAGTGGCTC ATTCCTGTAA 1200
TCTCAGCACT TTGGGAGGTT GAGGCGGGTG GGTCACTTGA GGCTAGGAGT TTGAGACCAC 1260
GCTGGCCAAC ATGGTGAAGT 1280
|
