| Tag | Content |
|---|
EnhancerAtlas ID | HS145-21350 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:137840370-137841250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr5:137841124-137841135 | AAAACAAAGAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27104 | chr5:137838886-137841876 | Esophagus |
|
| | 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 |
| GH05I138503 | chr5 | 137839081 | 137841522 |
|
Enhancer Sequence | ATTCACCAGA CAGGGTTTTA GACTTGATTT ACAGAGAACC CTTTAGGTGG TGAATTGTTT 60
TCACCTGTTA TTTCTAGTGC CTGCTATTCA GCCACATCCT CAGCAACTTG CAGCACCCAA 120
ACTGCCACAA AACAAGCAAG TAACTGTGCC CTGCTTCCCT AGCTCTAATC GGATGCTCCC 180
ACACCACTTG GCTGTTCAGT TCCTAGGTCC CCTGAGACCC AGTCCCATCA GGGCTGGACT 240
TGGCAGGCAG GAATCCCCTG GCATTCACTC AAGCTGGCAA CAAAGGAGAA GCTGGCATGA 300
AACTTAAATT CCACCTTGGC TCTCAGCCCT AAATCCACCG TGCCTGTCTG GGAGTGTCAT 360
GGCATGCGTC TTGGAGCCAG AGAACAAAAG ATGGCAAGTG CTGCAGGCCC AGACAGGCAA 420
GGACCACAGC CCATATATCC TGCACCACTG TGCTGCCTTC CAACAATTTT GTCTTCAAGA 480
ACAGCACCTA GACACGCATT AGGAGGGAAA ATTACACTTC CACCAGCACA GGCATGTTCG 540
CCCCTTCCCA GCTGGTAATT GAGTTTCGTC GTCAGAGCTA TCACCTAGAT CAGGTAAGAA 600
AATGGGTGAA AAGTACGCCA AGTGCCATTA CTGGTCAATT TTACTTAAAA CAGTTTTCTC 660
AAACCTGGAG AAAGCAAACC ATGCACCACC TTGGCTCCTC AACTAGGCTT CCTAAACTAC 720
CAAAGAGGCT CTTTAAGCAC CTCAACCTTG GGGGAAAACA AAGAAAACAA ATCCTCTTCT 780
GCTCTGAACC TGGCCTAGGA GCCCTGCTCC TCTGGACCAG CCCCTGACCT GCTTTTGGGT 840
GGGCTACTAC TCTCCTACCC AGTGTAAGGT ATGTAAGATG 880
|
