| Tag | Content |
|---|
EnhancerAtlas ID | HS060-18855 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:26266940-26267650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr2:26267433-26267451 | GATAGAGTTTCACTTTTG | - | 6.4 | | IRF9 | MA0653.1 | chr2:26267438-26267453 | AGTTTCACTTTTGTT | - | 6.15 | | LHX6 | MA0658.1 | chr2:26267407-26267417 | GCTAATTAGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09566 | chr2:26265610-26267925 | CD14 | | SE_28420 | chr2:26266415-26267505 | Fetal_Intestine | | SE_29154 | chr2:26266487-26267755 | Fetal_Intestine_Large | | SE_35193 | chr2:26266682-26267626 | HeLa | | SE_36382 | chr2:26266620-26267545 | HMEC | | SE_64640 | chr2:26266735-26267727 | 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 |
| GH02I026043 | chr2 | 26266536 | 26267906 |
|
Enhancer Sequence | GCACAATGGT GTGATACACT TAACACCTAC TGAACTGTAC ACATTAAAAA TGGTTAAGAT 60
GGCAAATTTA ATGTTATGTT TTAGAAAATG GTTTAAATGG TAAATGTTTT AGATATATTT 120
TCCCCACCGC TCAACAAAAC CCAAAAAACT AACACTCGAC CCAGTTCTCT AAAAGAGCAT 180
TTGATCACAG ACGGCCCCTC CTGTTCCAGG TGTTAGCTAC TGTTAACCAG TGGTTGTGAA 240
TCAAGAGGAT CCTTTATGGT ACTTTCCCAT GCTTTAATAT CACTGGTCTG TACTTTCAGT 300
TGTTGAAGGC AGATTTGTCT TTTTGTTGTC TGTATTTGCA TAGACCTTCT TGGAATGTTA 360
GAATCACAGA ATGTTAGTGC AGGAATGAAC CCTTAAATGA ATTTTCAAAG TGGGAAAACT 420
GAGACTGGTG AGGTGAAGTA ACTTCCAGAA GGCCAAAAGG CCACATGGCT AATTAGTTTT 480
TTTTTTTTTT TGAGATAGAG TTTCACTTTT GTTCCCGAGG CTGGAGTGCA GTTGCGTCAT 540
CTTGGCACAC TGCAACCTCC ACCTCCCGGG TTCAGATGAT TCTCCTGCCT CAACCTCCCG 600
AGTAGCTGGG ATTACAGGCA TGAGCCACCA CTGCTGGCTA ATTTTTGTAT TTTTAGCAGA 660
GACAGGGTTT CGCCCTGTTG ACCAGGCTGG TCTCAAACTC CTGACCTCAG 710
|
