Tag | Content |
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EnhancerAtlas ID | HS177-10000 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr17:79049770-79050560 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr17:79050506-79050517 | TGGGTGTGGCT | - | 6.14 | NR2F1 | MA0017.2 | chr17:79050197-79050210 | AAAAGGTCAAGGG | + | 6.39 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65309 | chr17:79049313-79050100 | Pancreatic_islets |
|
| 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 |
GH17I081073 | chr17 | 79047747 | 79050100 |
|
Enhancer Sequence | ATGCATAACG CAGAGAAGCA GAAGTGCCTG CACCCGGGTG TTCCCTCTTG CTAGTAATCC 60 TGAGGTTTGG TAGAAGCCAG CTCCTGCTGG GGTCAGGGGC AGTGAGGCAG GGGCTCCCCA 120 GAGTACAGCC TGAGAGGCCT GGCTGCTTGG CTGGGGGGAG TGCCGAGTCT CAGGTCCTGC 180 CGGGAGGCAC AGTCCTTCCA GAATCAATCC CTGTTACCAT CTGCAGCTTA ACTCATTTTA 240 AGCTTAACCA TCTGCAGCTT AACTCATTCT TGCTTTATCT TCCCTGTGGA CCAGGTCTAG 300 CCTGGGGCAG ACAGGAGATG GCAGATGGAC ACCTGGGAGG GGCTCACTGA GCTCCGCCTC 360 TCCATCAACG GAGGCCCCGT CTAGGTTGTG GAGGATGCTT GAGAGAGCCC TGATGTTCTG 420 ACCTCCCAAA AGGTCAAGGG TGCTGGCAGC CGGTGAGACG CCGCAGTTTG CTCTGCTCCC 480 CGGGGCTGTG CTTGCCAGGA GACATTTCGG CTATAAGCAG GCGAGAATAC CTCCAGAACA 540 CACATCAGGA AGACAGATGG TGTGCAGGTG GGGCTCAGGG CTGTCATCCC CTGAAGCTGC 600 TTCTGAAAGA GCTGTTCTTG CAGCAGCACT GTTACAAAAG GCCACATGGG AAACAGCCCG 660 CACCTCTCAG TGGATGCCGG CAGAAACGCC TCGTGTATCC ATAGGGTGAA GTTGTATTCA 720 ACCACAAAGG ACAGGCTGGG TGTGGCTCAT ACCTGTAATC CCAGCACTTT GGGAGTCCAC 780 TTGATCCCAG 790
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