| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15080 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:99221090-99222240 |
Target genes | |
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_18352 | chr13:99217854-99229137 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19168 | chr13:99215019-99222260 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_23248 | chr13:99221550-99222012 | Colon_Crypt_1 | | SE_24027 | chr13:99221643-99221949 | Colon_Crypt_2 | | SE_24799 | chr13:99221363-99222009 | Colon_Crypt_3 | | SE_27165 | chr13:99221134-99222152 | Esophagus | | SE_27798 | chr13:99219943-99225366 | Fetal_Intestine | | SE_28780 | chr13:99220199-99229372 | Fetal_Intestine_Large | | SE_45616 | chr13:99221084-99225931 | Osteoblasts | | SE_50450 | chr13:99221031-99222245 | Sigmoid_Colon | | SE_52580 | chr13:99221175-99222143 | Small_Intestine | | SE_54177 | chr13:99221187-99222138 | Spleen | | SE_62949 | chr13:99214776-99230836 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCAGCCTGGG TGACAGAGCG AGACTCCATC TCGAAAAACA AAAAAGATAA AAGAATATTT 60
GAGGGCCGAT GCAGAAGGTT CACCATCCAA GTAATAAAGT TTCAGAAAGA AAGAACACAG 120
AAAATGGAAG GGGGGAGGGG AATCAAAGAA AAAAGTCAAT GAAAAGATCT GAGTCGCTTC 180
ACAGAAAAGG CCTAACCAAG TATCTGTCAC GAGAAACGAA AACAGCCCCA CTCCAAGCCA 240
CATCATTGTG AAACTTCAGA ACTCAAGGAA AAAGTTCAGA TCCCATTAGG TCCAGGAAGA 300
ACAGCACAGC CTGCACACAC AGAAGCCGGT GCTGGCAGGG CCTCCATCTT CAACAGCAAC 360
ACTGGAAGCT AAAACACAGT GGAGAAACAC CTTTAAAATT CTGGAGGAAA TGAATGTCCA 420
CCCTGCAATT TTACACCATG CTAAAATATC AACTGAGGGA GAAGAAAAAA AATTTTTGAA 480
AAGCCTGTCT CCCACGCTGC CTATTCACAG AAAATGGCGC ACTATATGCC CAACCAACAT 540
CATGGCATAA ACCAAGAAAG AAAATGACAG CAGAGACAAA AAAAAAAAAA CAAAAAAAAA 600
CAAAACAGAT ATTCAACACA AGAGAGCAGC AGAAGGAACC CAGAGGATGA GAGCAAAGGA 660
AGACCAGAGG ATGGGGGTGG CACAAGAAGC ATAGAAGATA CGCAGGTGAC GAAAGGCACA 720
GGTGCCACCC GAACTTCCTA AGACAAGGTT GCAACAACTA CAGAGTGCTG GGATGAATGA 780
GAAGCATTAC CAAAAGAAAA GAAATCTGAT CAGTAACTAT GGTTGAGTAA TAATGGCTGG 840
GCTGCAGATC CGTCTGCAGT CCATTAATGT ACACACCGCA TTCTGACCTC ACTGACATTA 900
CAACATCTCT CTGCTGGGGG AGAGCGGGGA GCCCATGTGA GGAAAAGAGG CAAGCGGAAG 960
AGAAGTAAAT CCTCATCCGC AGGGTCCAAA GTCTATAGAC AATGCCTGAA ACCAGGAAAA 1020
AAAAAAAAAC ACAGGCAGAA ATTTTTTTTT TTTTTTTTGA GATGGAGTTT CACTCTGTCA 1080
CCTAGGCTGG AGTGCAGTGG CACCATCTCA GCTCACTGCA ACCTCCGCCT CCCAGGTTCA 1140
AAGAATTCTC 1150
|
