| Tag | Content |
|---|
EnhancerAtlas ID | HS046-12522 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr15:67366800-67367990 |
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 | CTGCACTTGA TTGCGTAAGC ATGAGCCTTT TGTTAGGCAG CGTGGATGTT GCAAGTTTAA 60
ACCCCAACTA GGAAATGAAA AGTGAGTTTC CTCCTAAATA GTTCTTTTTC AGTATCACAT 120
GGCTCTCCCA GCTTACATCT GGCAAGTTTT TCTCTTGAGT GCTTTGCCGG TAGTTTAGGA 180
CTCCAGTATT GTATTGTATT GTTTGTTTGT TTCTTTATCT CTGTCTCTCT CTTTTTTTGT 240
TTTTTGAGAC GGAGTCTTGC TGTGTCGCCC AGGCTGGAGT GCAGTGGCGT GATCTCAGCT 300
CACTGCAACC TCCGCCTCCC AGGTTCAAGC AGTTCTCCTG CCTCAGCCTC CCATGTAGCT 360
GGGACTACAG GCGCCCGCCA CCATGCCCAG CTAATTTTTG TATTTTTAGT AGAGATGGGG 420
TAGGACTCCA GTATTAAGAA ACACTGTGTA TGGCTTTGCC TTTGAAACCT ACAGAGTTAT 480
GAATCTGGTC CCTTTTGCTG CTAAGTGTTG CATCACAAAC TGCCAAGCCA AGTTGTAACT 540
CTGAGGTGTC ACCATTTTTT TTTTCTTTTC AACTGGACAT TTGAAAATAG TAATGCTTTT 600
TGGGTGTGTG TTTTTTAAAG GTCTGTTTTT ACGCTGTCAC TGCTCAAAAA TGCCAAAAGG 660
CATTTTTTCC TTAAAAAATC ACCTCTGGGC TAAGCCCAAA TGTGGAGTAA TGAATCCAGA 720
AAGGACTTTT TGAGTAGTTA CAAGTGGCTG AAAGCAGGCA CTGGTGATGG AAATTGGGTT 780
TTTCCTTTTG CTTCAAATCT TCCTGGTTGT AAACTTTTTC TTACCCTTAT TGAAGTCAGA 840
CTCAAGGTGG GTCTAATTTC TCCCAGCCCA TGGGAAGGCA GAGTGAATTA CTGCTTGTTG 900
TGCCAACCCT TTACATTTTG TGTGTGGCTG TTTGTCTCTA CCCAGACAGG TTCTTCACAT 960
ATTACCTGGG GAGCAGGAGA GGGGGAGGAC AGGAAGAGCA CAGTTGGGCA GAAAGAGCAA 1020
AGCCTCTCAA GTCTGATGGG TTTGGGTTTG AGTCTGACAG TTATTAGCTA TGTGGTGACC 1080
TTGGGTACTT TGCTTCAACT TATTGAGCCC CAGTTTCTGC ATCTGTAAAA TGAGGATGAA 1140
ACTACCTACT TCATAGAAAT CAACCCAAGT GGCCGGGCAC GGTGGCTCAT 1190
|
