| Tag | Content |
|---|
EnhancerAtlas ID | HS116-10005 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr13:99125630-99126900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZIC3 | MA0697.1 | chr13:99126699-99126714 | GACCCCCAGCTGTGC | + | 6.17 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27318 | chr13:99125624-99126422 | Esophagus | | SE_32245 | chr13:99125599-99127531 | Gastric | | SE_45616 | chr13:99125684-99126805 | Osteoblasts | | SE_65772 | chr13:99125363-99126243 | Pancreatic_islets | | SE_65772 | chr13:99126270-99131228 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 99125746 | 99126400 | | chr13 | 99126463 | 99126900 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I098473 | chr13 | 99125593 | 99126985 |
|
Enhancer Sequence | GTGTCATCCA ATGAGTTAAG AAACATGGGT TCTAGTCTCA GCCTTGCCAA AATCTACACA 60
GATGAACTTT GATAAATGGG GTCAGCTTAA AATAAAGAGA ATGGACTAAA CATGTAAGTT 120
CCTGGTCGAG TCCCAAAATT ACATGACCCC AGGAAAAGGG TCAACAGCCA AAGTGACTGC 180
AGATGAGAAG CAGCCAAGGC AGTGTCCCTC CCACGTGGGG TAGAGACACT CCCAGGCAAG 240
GGCACACACC CAAGACCAGC CAGGTCTGCT GTGTGGGTAT GTGGGGGGTG GGGGAACCCA 300
TCAGTCACTC ACCAGCCAGA GGCTGTCAAG GCCATCATAG TGCTCAGAAA AGTCACAGCC 360
ACCGCTACCA CTCAACAGTG AGACGGGCTC ACTCCTCCCA AGGTGGAACC AGGTACGCCT 420
GCAACTTGAG CTACAACCTG GACGCTTTCT AACAGTCTAT AGCTTGCAAC GGTGACCTGG 480
GTCTGCAGGG AAAGTCACCT GGTGCTTCCT GTACTATGTT TAACAAGGTG GGAAGTTTAC 540
TGGGTACTGG GAAGATTTCT GTTTAAAAGC AGCAGCAAGG TTCGGCCTAT ATGCATATCT 600
GAGTTAGGTA TTTGTTTGCT CAGAAACTTG GAGCCCAGGA AAGCCAATTC TCCGTGGATC 660
ATGTGGCCTT TTAACTGTGT ACAGGGTCCT AAGAAGAGCA GACTGTGCGA ACTGAAGTTA 720
AACCAGAGCC CTAGGAGGCA AAGTCCCGGG ATTTTTTGTC CCATCTAACA GAGTTCACAA 780
AAGTGGAGGG CAACAGAGAA AAAGAATATG AGAAAAATTA GGAGAGTGTC CCTAACACAG 840
GACAAGTAAA AAACAGTGGG AAGAAAGGGT TAGGGTTTCA TCACATGTTG ACAAGGACAG 900
GCTGGGAACG AGAATCCTCA GAACTAAAAA TAATAGGAAG ACCCTGCAGC AGTCACTCAA 960
AGCACTGTTC TTCCTCCATT CTCACGCTTC CGTGGACTCC CTTTCTCTTG TGGGAGCCCC 1020
TTTCTCTACA GGCCCCTTCA AGGTTGCCGA TTCCACGCAC TTGCACTTCG ACCCCCAGCT 1080
GTGCCCAGAC AGCAGGTGGA GCCCCTCTGC AACCGCACAC GCCTCCACCC CTCACCACCA 1140
TGGCCCTTCA GTTCCTCCCA CCCCCCTCCA AACCCGCTCC ATCCTGTGTC CCCGCTGCCA 1200
CCAAACAAAC ATAGCCTGAG TTAAAAACCT CGATCATGGT GGGCTGGATC AGCACAGGGT 1260
ATTAAATGAT 1270
|
