| Tag | Content |
|---|
EnhancerAtlas ID | HS116-12080 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr15:67366840-67367850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr15:67367000-67367012 | GTTTGTTTGTTT | + | 6.32 | | Nkx2-5(var.2) | MA0503.1 | chr15:67366953-67366964 | CTTGAGTGCTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00035 | chr15:67366306-67369231 | Adipose_Nuclei | | SE_09181 | chr15:67366082-67371152 | CD14 | | SE_10181 | chr15:67366164-67371299 | CD19_Primary | | SE_10875 | chr15:67354078-67404812 | CD20 | | SE_13896 | chr15:67366254-67367429 | CD34_Primary_RO01536 | | SE_18371 | chr15:67364370-67371368 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20091 | chr15:67366215-67368054 | CD56 | | SE_25827 | chr15:67366966-67368215 | Duodenum_Smooth_Muscle | | SE_28551 | chr15:67366315-67367413 | Fetal_Intestine_Large | | SE_34728 | chr15:67366732-67370465 | HeLa | | SE_36917 | chr15:67364416-67376637 | HSMMtube | | SE_37941 | chr15:67366127-67370517 | HUVEC | | SE_42172 | chr15:67367423-67368030 | Lung | | SE_44749 | chr15:67366247-67368098 | NHLF | | SE_45534 | chr15:67364411-67371470 | Osteoblasts | | SE_47100 | chr15:67357928-67475420 | Panc1 | | SE_48052 | chr15:67366504-67374901 | Psoas_Muscle | | SE_51081 | chr15:67366276-67376636 | Skeletal_Muscle | | SE_52344 | chr15:67366725-67368051 | Small_Intestine | | SE_53518 | chr15:67366754-67367448 | Spleen | | SE_55686 | chr15:67367227-67369589 | u87 | | SE_58377 | chr15:67342858-67447290 | Ly1 | | SE_59897 | chr15:67354926-67408793 | Ly4 | | SE_60508 | chr15:67357006-67428179 | DHL6 | | SE_61631 | chr15:67357404-67427415 | Toledo | | SE_62286 | chr15:67356723-67443338 | Tonsil | | SE_67502 | chr15:67367227-67369589 | u87 |
|
| | 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 |
| GH15I067072 | chr15 | 67364341 | 67371314 |
|
Enhancer Sequence | CGTGGATGTT GCAAGTTTAA ACCCCAACTA GGAAATGAAA AGTGAGTTTC CTCCTAAATA 60
GTTCTTTTTC AGTATCACAT GGCTCTCCCA GCTTACATCT GGCAAGTTTT TCTCTTGAGT 120
GCTTTGCCGG TAGTTTAGGA CTCCAGTATT GTATTGTATT GTTTGTTTGT TTCTTTATCT 180
CTGTCTCTCT CTTTTTTTGT TTTTTGAGAC GGAGTCTTGC TGTGTCGCCC AGGCTGGAGT 240
GCAGTGGCGT GATCTCAGCT CACTGCAACC TCCGCCTCCC AGGTTCAAGC AGTTCTCCTG 300
CCTCAGCCTC CCATGTAGCT GGGACTACAG GCGCCCGCCA CCATGCCCAG CTAATTTTTG 360
TATTTTTAGT AGAGATGGGG TAGGACTCCA GTATTAAGAA ACACTGTGTA TGGCTTTGCC 420
TTTGAAACCT ACAGAGTTAT GAATCTGGTC CCTTTTGCTG CTAAGTGTTG CATCACAAAC 480
TGCCAAGCCA AGTTGTAACT CTGAGGTGTC ACCATTTTTT TTTTCTTTTC AACTGGACAT 540
TTGAAAATAG TAATGCTTTT TGGGTGTGTG TTTTTTAAAG GTCTGTTTTT ACGCTGTCAC 600
TGCTCAAAAA TGCCAAAAGG CATTTTTTCC TTAAAAAATC ACCTCTGGGC TAAGCCCAAA 660
TGTGGAGTAA TGAATCCAGA AAGGACTTTT TGAGTAGTTA CAAGTGGCTG AAAGCAGGCA 720
CTGGTGATGG AAATTGGGTT TTTCCTTTTG CTTCAAATCT TCCTGGTTGT AAACTTTTTC 780
TTACCCTTAT TGAAGTCAGA CTCAAGGTGG GTCTAATTTC TCCCAGCCCA TGGGAAGGCA 840
GAGTGAATTA CTGCTTGTTG TGCCAACCCT TTACATTTTG TGTGTGGCTG TTTGTCTCTA 900
CCCAGACAGG TTCTTCACAT ATTACCTGGG GAGCAGGAGA GGGGGAGGAC AGGAAGAGCA 960
CAGTTGGGCA GAAAGAGCAA AGCCTCTCAA GTCTGATGGG TTTGGGTTTG 1010
|
