| Tag | Content |
|---|
EnhancerAtlas ID | HS007-07412 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:74409850-74411660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr17:74410388-74410402 | AAGACAAGACAAGA | + | 6.34 | | Sox3 | MA0514.1 | chr17:74411494-74411504 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65659 | chr17:74410140-74411765 | 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 |
| GH17I076414 | chr17 | 74410478 | 74410930 |
|
Enhancer Sequence | CCAACACAAA ACCCAAGACC CACACAGTCA CACTCAGGCA CTTTTAGGGT GAGGAACTTT 60
AACTTTCTGA CCTGACTTAA AATGTTACTA AATTGGCTCA AACAGTAAAA CCAGGAGAGG 120
CAGAAAATGG GGCCTCCTGT TGGAGCTGGA CTCCTCTTCC AGCTTCTTCC TAAGCCCGAG 180
TTTCCAGTTT GGACTGGATT TGAGGATGTG AATGGTCAGT AATTCCGGCT GGTGCCAGTG 240
TAAGGACTTT CTCAGAGCAG TTGACCATCA TGTGGCTGAG CCCTGATAAC CCGGCAATCA 300
GCTCACTGCC CACCTGAGGA CAGAAGGTTT TACCAGCAAA GCACAAATGG CCAGGGGGCC 360
TCACATGCTT GGGGGAGGGG AGGGAGAACC TCCGGAAATG GCTGGAAGTA AAAGAAATGT 420
TGGTGCCCCT AGCTGGAAAA TTCTGTCAAT CATGAGCTAC GGAAGCCATT CAACAGAGAA 480
GCTGTGCTAA GACTGAGGTC AACTGATTGA ATAGTTTTTG AGTGTTTTCT ATAGACTTAA 540
GACAAGACAA GAATACAAAT ATATAATTAA GAATGGGAAT TAGCTTTCTA GAACTTACAC 600
TGAGATGAGG GAGGTAAGAT GAAATTACAC CTGAAAACAG TTATACACAA GTAAATAGAG 660
CACTAAGCTG GGTGGGGAGA CCAGAAACTG AGTCCTGTCT GGATGGCGGT GGGGGAAGGC 720
AGGAGGACCG GGGTTGCAGG GGAACTGCAC ACCAGGGACA GCCCCCACGC CCTCACCCCT 780
GACACCCTCT CTGATCTCAC AACGCAGACT CTCAGGCTGG GCAATACAGT GCTGCTGCAT 840
CACCGCCTGG AAACTCGGCT GCAGCTCGCC AGCTTGCTGG AATGGCCTGG AGGCACAGCC 900
TGCCCGAGGG ACAGAGAAAG GGGACTGAGT CCAACTGCCT GCTAAGTGAG GGGGAAGGAC 960
TGCAGAGCTT GGCCTGGCAG GGGGCCAGCG GGCTGGTCTC TGCAGATGCT GCGGTGTTTG 1020
ATAAGCAATA TGTGCACTTG GCGGCAGGAG CTGGGAGCCG AGGAGCCCAG CCCTGCACCC 1080
CTCTGTCTTG GCTCTGGGCT TGTCAACCTG GCTTAAAAAA AGACAAGAAC AGCCCAGGCC 1140
TGGCTCCTGC ATTTGAAGGG AGGGGACAGA TGGGCATCTT TAGGAGAAGG CCGCCTCCTT 1200
CCTCAAAAGT ATAAGTAGAA GGCAGAAAAG TGATCAGCAT GATTCCATGT TCTGTTCTTG 1260
TCAGGCCTGA CTGGGTATCA CTACCTAACC AGTGGCCCCG GACTGCTCCA TTTCAGATGC 1320
GACAGGCTGC GGTCCTGTGG CTGCCGGGCA TCCCTGAGAA CAAGAAGGGA GTCGGCCAGC 1380
TGGCCAGGCA CAGAGCAAGT TCACAGCCTC AACACCCCTC AGTGTCTGAT GCCATGTTAG 1440
TTCACGGAAT GAGGACCCAG GCTGCTAATC ACACAAACTG ATCCTGACGG AGCCTGCCAG 1500
GAAAGAACCC CACGTGCACT GCCTCTCCCA ACCCTATGAC CCCCACGAAG GAGGCACCAC 1560
TCTTGTTCTC ATTCCACAGG AGACTGGGTG GCTTGGAGAA GTAAGTGAGC TGCCTAAGGT 1620
CACCCAAGTG CCAGGACTCC AGAGCCTTTG TTTTGCTCAC CTGCCCTTCC TCATTTGACC 1680
TGTCTGGTCT CCAAGCATGG CCCTTGCTAC ACCTGGACCA ATTGGAACCA TGCTGCCATT 1740
CAAGTGTGGC CCTGGGCCTG GCGAGGTGGC TCACACCTGT AATCCCAGCA CTTTGAGAGG 1800
GCAAGGCGGT 1810
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