| Tag | Content |
|---|
EnhancerAtlas ID | HS176-28729 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr4:26016350-26017510 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr4:26017366-26017376 | ACCACTTGAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_44578 | chr4:26015538-26019579 | NHDF-Ad | | SE_46071 | chr4:26014391-26019474 | Osteoblasts |
|
| | 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 |
| GH04I026014 | chr4 | 26015892 | 26018452 |
|
Enhancer Sequence | GGGCAGACGG AAGTTTTCCT CCCCTCTTAG GGACCAACAG GCACTTGGAT CTGTACTATG 60
AGAGGACAAG AAGCCTGGAA AATGTCATTC TGAGGGAGGT TCATGGCCTC TGGTACCATT 120
TTCGAGACAT GGGTTCAAAG GTTCTGTGTC ACATGGCATT CTGCCAGGGA GGTGGGAACT 180
CTCAGCTCAA GCAGTAGGTG AAAAGCCCTC TCTTGTTTAA GCTTCAGTTT CCATAATTTT 240
TGACAGGATC TCATGGGAAG AATTTAGTGG CAGAAATAAC TTAGCGGAGA TCATCCCTTC 300
CTGGGGTGGG AGTCTTAGTG GCAGTTACCA GCAGAAAAGC TAATGGGGTA ACCCGAGAAA 360
TCTTCCTGGA GGAGGAGATG TTGGCTGAAT CATCGATCAG CTCATATCAC TGAGCCAAAT 420
GCTTGTCATT GGCTTTGGGG GGGCAACGTA GGGCCCACAG TTCCCCTCAT CATCCTCAGA 480
GTTGACACTC CCCAGTGCCT CACAGAGATG ATTTCAGGGT TCAGAAATTC TGACTCCCAA 540
CCCCCTTGGG TCCACTTCCC CTCTTATCAT GCAGGCCATC TCCCCGGTCT TGGCTTACCC 600
TGTGACCACA CTGCATTCTC CTTCCACATG CCCTGACACA CGCTCTGAAA TGCCAGGGTT 660
CTCATGAGTC CAGCCTGCCA GGAGCAAGGC TTGCCAAAGC TGTGTCCCAG CCAAGCGGGT 720
GGCCTGCGGA GTGAGCCATA GGACTGCATT CAGCCCAGTT CCAAGCTGGA AGGTGAGGGC 780
AGCCTCCCAA CTATTTCTTC CAACCTCAGA AACGATTCAG TGCTGGCAGT TCACACGAGG 840
TCCCCCTGAC ATCTCCAGTC AGGAATGCAA CTTGCTGTGG ATTCTGAGGC AAAGAGAAGA 900
CCATTAGGAA GGAGGGAAGT CATTAGCAGA TGGGATGACC GGCATGCATG AGAGACACAT 960
CTGCCTTTCC CTGAGGTGCC CAGGGGCTTG TGTGTGGAGC CTTCTGGGAC TCTCTGACCA 1020
CTTGAGACCC AGAAGATCAA AGGTCTGGTA GCCACGGCCC GCTTTGAATC CATAATTCCT 1080
TGCCTCTCAC AAATGAAGGG AAGAAAAGTT GTCAGGAGGC AAAGCTGTAG CTAGCAGTTT 1140
GGCCAACATG CATGGATTGT 1160
|
