| Tag | Content |
|---|
EnhancerAtlas ID | HS073-07499 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:18949390-18950830 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr19:18949708-18949723 | TTCTATTTTTATCAC | - | 6.61 | | PRDM1 | MA0508.2 | chr19:18949654-18949664 | GTGAAAGTGA | - | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24551 | chr19:18950279-18950943 | Colon_Crypt_2 | | SE_41842 | chr19:18950120-18952058 | LNCaP | | SE_65715 | chr19:18949496-18953573 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I018838 | chr19 | 18949741 | 18949910 | | GH19I018839 | chr19 | 18950067 | 18951699 |
|
Enhancer Sequence | AGGTTGCGGT GAGCTGAGAT TGTGCCATTG CACTCCAGCC TGGGCAACAA GAGCAAAACT 60
CCATCTTAAA AAAAAAAAAT GCTCATGACT TCATTTTGGC TTTTTGAATC CTCTGGTAGC 120
CCAGGTGTGG TTTTAGGGTG CCAGAACATT GGAGATAAGA TGCCGTTTAC CTGGAGGAGT 180
GTTGGCAAGT GTTTGGTCAG CACTTACCCC TTAGTAGACT TACTGAGTGT GTTTTCAAAT 240
TGTTAGGAGT TTCCCAGTGA TTATGTGAAA GTGACCTGAG CTGACACTTT ACAGTTAGTG 300
GTGAATACAC GAAACAATTT CTATTTTTAT CACAATTAAT TACCCGGATT CAGGATGACG 360
GGGTGGGGGA TTATGACTAA TACTATACCA GGACTAACTA AAAAAAGAGT TCCCTCTCAG 420
CCTAGCTACC ACCACCACAA AAGCTTACCA CCATCAGCTA CCACCACATT TCTCTCATTG 480
CTTGATTGAA GTCTGATGAC CTACCAGGGA ACCCCCTTCT TTTCTTTTTA GACGGAGTCT 540
CGCACTGTCG CCCAGGCTGG AGTGCAGTGG CGCGATCTTG GCTCACTACA ACCTCTGCCT 600
CCCGGGTTTA AGTGATTTTC CTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGGTGCGCA 660
CCACCATGCC CAACTAATTT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA CCATGTTGGC 720
CAGGCTGGTC TGGAGCTCCT GACCTCAGGT GATCTGCCCA CCTTGGCCTT CCAAGGTGCT 780
GAGATTACAG GCATGAGCCA CCACACCTGG CCCCTTTAAG TATAGAACTT AGTGCTGTTT 840
TAGTAAATTT ACGGAATTGG GCAGCCACCA CAGCAGTGCC TTGCTGTCTC TGATTTCTCT 900
TTCGCTCCTT TCCGCTCCCT CCCCACCACC CCTTGTCAGA CCCTGTGCTC ATGCCCAAGG 960
TCACCCGTTA GGGAGGTGTG TCCACCGCCT CAGACTGAGC CCTGCCCTGG GGAGGTCAGA 1020
AACATGGCCA AGCCCTGGCC CCATGCTCCC CCGCCTTTAA GCCCCGTGTC TGTTAACTTT 1080
TGCACCCTCT GCGAGCTGCT GGGCAACCTC TTCAGCCTGG CCCTGGACTT CAGCCATCCC 1140
CTGCTGTTTT CTTACTTCCT GGCCTTGCTG TGCTTGTGGG ACTGAGGGCA GTGAGGCCAG 1200
CAGAGGGAGA GTGAAGCCTT TGACCCCCGC GGTTGCACTG TTAGAAGACA GCACATGCCG 1260
CCTGGCCAGG GTGCTGTGAG GGCCCCAGGA GTAGGAGTGG GCTCCCCTGC TAAGGGAAAG 1320
CCTGTGGGAA TGGCGCCTCT GGAGTTGTTC AGAAGCTGTA CCTGCCAGGC AGAGGGGTGG 1380
GCACAGCACT TTGCCTAGAA GGAGGGAGGG TGGATGTGGG GCCAGTGGGG CCAGGGCAGG 1440
|
