| Tag | Content |
|---|
EnhancerAtlas ID | HS182-07330 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr15:67369620-67371250 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 39 | ID | Coordinate | Tissue/cell |
| SE_02047 | chr15:67369842-67370778 | Aorta | | SE_09181 | chr15:67366082-67371152 | CD14 | | SE_10181 | chr15:67366164-67371299 | CD19_Primary | | SE_10875 | chr15:67354078-67404812 | CD20 | | SE_14469 | chr15:67368065-67370713 | CD4_Memory_Primary_7pool | | SE_17822 | chr15:67368660-67371356 | CD4p_CD25-_CD45ROp_Memory | | SE_18371 | chr15:67364370-67371368 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19163 | chr15:67368109-67370952 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_23212 | chr15:67369614-67371249 | Colon_Crypt_1 | | SE_23998 | chr15:67369744-67370844 | Colon_Crypt_2 | | SE_23998 | chr15:67370943-67371252 | Colon_Crypt_2 | | SE_25827 | chr15:67368302-67371308 | Duodenum_Smooth_Muscle | | SE_26536 | chr15:67369832-67370882 | Esophagus | | SE_27694 | chr15:67369393-67371461 | Fetal_Intestine | | SE_28551 | chr15:67369321-67371497 | Fetal_Intestine_Large | | SE_31411 | chr15:67369701-67370930 | Gastric | | SE_32497 | chr15:67368255-67371005 | GM12878 | | SE_34355 | chr15:67368112-67369800 | HCT-116 | | SE_34355 | chr15:67369821-67370682 | HCT-116 | | SE_34728 | chr15:67366732-67370465 | HeLa | | SE_36917 | chr15:67364416-67376637 | HSMMtube | | SE_37941 | chr15:67366127-67370517 | HUVEC | | SE_40033 | chr15:67368138-67370877 | K562 | | SE_42172 | chr15:67369741-67370838 | Lung | | SE_44149 | chr15:67369632-67370642 | NHDF-Ad | | SE_44749 | chr15:67368688-67371076 | NHLF | | SE_45534 | chr15:67364411-67371470 | Osteoblasts | | SE_47100 | chr15:67357928-67475420 | Panc1 | | SE_48052 | chr15:67366504-67374901 | Psoas_Muscle | | SE_50064 | chr15:67368620-67371374 | Sigmoid_Colon | | SE_51081 | chr15:67366276-67376636 | Skeletal_Muscle | | SE_52344 | chr15:67368168-67371321 | Small_Intestine | | SE_53518 | chr15:67369913-67370745 | Spleen | | 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_64236 | chr15:67369816-67370788 | NHEK |
|
| | 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 | GTTGCGTGGC CACAACTGAA TCCCAGTCCA GGTGGCACCA TTATATGGGT AGCATTTTGG 60
AGATGTTCAC AGGAATTGAT TTCCCTCACC CTCAACCCAG GCCAGAGTGA ATTTAATGCA 120
GATGAGGGAG AAGGTGCTAC ATATTATAGC TGCTCATTCA AAAAGTGGAG CAGAGAGCTG 180
GACCACTGAA TGTGCCTTTG TTTGCTGGAA ATCTTTATTA AGTACCAGAG ATATAGAGAT 240
GAAGTTGTGT CTCTGAACTG CTCAGAGGCA AAAAAGGGAC ACCAGTAACC ACAGTTATGG 300
TGGGCCTGTG GAAGAGACAC TATAGTGAAG GTCAAACAAA ATATTTGGGA GCCTAGAGGA 360
AGAACAGGTC TATTTCTGGA GGTATCAGAA GGCTTCACAG AGGAGGCAAT ACTCAATTGG 420
GGCCTTGAAG GATGGATAGG AGTGTAGGAG TGGAGTGGGA GGCAGCACAG AGCACAGACC 480
AGACTGCGGA AGGGCCTGAC ATCTAGGGAA GGCAAGACAG TTTAGGGTGG CCAGAGTGTG 540
GATGAGGGAG TGGCCAGAGA GGAGTTGGAG AAGGATGTTG TCAAGGGCTT TGGCTTGCCA 600
AACTTCGTAC TTTGTGTTTG GACCTTGCTC TGTAAGTGTC CAGGAGATTT TAAAGCAGGG 660
GAGTGGCACG GTGAAAGCCA CCACTCTATC GTTTCTTGTT TCATTTCCTC CTCTTACCCA 720
GTGGCTGTTA ACAGCAGGTT TTCTGCCCGA GTTATCCAGG TCAGAGTCAT AATCCCTTAC 780
AGTACCATGT GGACAGCTTT AGGCTATGTC TGGAGCAGGT TGAAGATAGT GTTTTGTTCA 840
CTGTCAGGAG AGAAGACATG TTGTTCAGCC AGGAGGGCTC AGGGACCCCA GGCGTTCAGG 900
TAATTAGCCA GTGAGTCATG TCAGGCTTTT GATATGGATA CCTTGGGAAA CTAAGTGGGG 960
TGTTGCTGGC CTCCATGCAG ATGCCTGGTC TACCCAAGCA CAGGCCCCCA AATTAGATCT 1020
CGGCCTCTGC TGGGTCTTCC CTGTGCCTGA CACAGTGCCT TCATATGGAC CGTCTCTGGT 1080
CAGTGTTTTC AATTTCTTTG TTGATGATCA TCAATCAAGG CCAGGCTTTC CAATTCCAGA 1140
CCACACTGCA ATCAGTGGAA ACTACCTAAA TTCAGTACTG CAGACCCATA GCAGGATGTA 1200
TGTTTATTGA AAACAGATTA TATTCCTTAA TGAGAGACTA AAACAGCATG TTTAAATCAG 1260
TATTCTTCAT TCCTTTTATC ATTGAGAGAT TGGTTATTAT TTACCTCGCC TTTAGAGGGT 1320
CAGCTTGGTG GTGGTGGTGG TGGTTTAAGT TGCTGGGTTT TTAAAAGATT GAGTTTCATG 1380
TCCAAGGACT GATTCTACTT CATGGGCTGT TTTTGAAAAC ATTGCTAGAA ACCTCTTAAC 1440
TGAAGGCAAG ACCAGGGGCA GCCTATTGCT GCGGAGTGCC CTGGGTTCAA ATCCCTGCTC 1500
CCCAACTTAC TGCGGTGGTG ACTGTGGACA TGTTGTTTAA CTTATTTGAG CTTCCTTTTC 1560
CTCATCAGTA AAATGGGAAA AACAATGACC TCCCTCAAGG AGGGATGTTA TTGAAGTTAT 1620
TTACTTAAAT 1630
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