| Tag | Content |
|---|
EnhancerAtlas ID | HS176-24874 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr22:19998030-19999420 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr22:19998462-19998474 | GGCCACGTGCCT | + | 6.07 | | STAT1 | MA0137.3 | chr22:19999314-19999325 | TTTCTAGGAAA | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_21038 | chr22:19998264-19999336 | CD8_Memory_7pool | | SE_40159 | chr22:19996708-19998877 | K562 | | SE_41259 | chr22:19997310-19998999 | Left_Ventricle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 19998277 | 19998386 | | chr22 | 19998724 | 19999021 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I020010 | chr22 | 19997469 | 19998770 |
|
Enhancer Sequence | CCTGCAGGGA AACCAGAGGG CATGAGTGAG GTCAATCCAG CTGGGTAGGT CCCTGCCGGA 60
TAAAGGTACA CAAGCCCAGA CCGTCCTCTA AGCAGGACCT TGTCATGCCT GATCTGAAGG 120
TCATCCCGTG GTGCTCCTGA CTCATAACCA CACACTCATG TGTACCTTCT TGCCCCCACA 180
TGTCCAGGAC TGTAGGTGAC ACTGGGCTGC CACGGTTCCT TGTCAGCATG TCTAATGCTG 240
TTGACCATCC TTCAGAAACG TGATCCTTCA GAGATGTGGA CTGATAATGA CGTCTTCCCC 300
ATCACACACA GCACAGCAGT ATTCCCACCC CAGGGTAGCC AGGCTCAGGG TCCTGTTGCC 360
CCACGCAGGT GCTCACAGCC CCATAAGACA TCTGCTCCAC CTCCCTAGAG TCCGCTCCCG 420
CCTTGTGGGC GAGGCCACGT GCCTCTCCTG AGGTTCCCTG AGGCCAACAT AGATCCTGGG 480
CCCTCCCAGG CAGGCAGCTG CCCCCAACAG TCTCCAGTAC AGGGAGGGCG GGGAAGCAGG 540
CAGGTTCCTG GCCCTGGAGC TGTGGCCAGG TGTGAATAAC CATTTGTCTG GGATGGGGGA 600
CCTGGCACTC AAGCCTGGGG AGCTGAGGCT TATGGGCTGG AGCAGGAGAC AAGGGGGTGC 660
CTGTACTCAC ACAGCTTTCA GCCTTCCTCA GGGGAGGACC CTGCGGCTTC CTGTCTCAGC 720
TAATGGCCCC GGGGACACAT TCCCTCTCCT TATATCTAGG CCCGGGGATA TTGCCAGAGT 780
GTTCATGTCA TAAAAATGAA AAACAGGACA CTGCAGACAG ACAGGGAAGG GCTGGGCCTC 840
GGATGGGAGG CTGTCTCTGG GGGACATCGG TAATGAGAGC TCTCTCCCCC GCCTCTACGG 900
TGTTTTCTAG ATTGTTCTGA GGCCCCGCCC AATAGTCCTT TGTGGTCATG GTCCATTCTG 960
GTGCCCCAAC GGTGTGTTTC CCCGTCTCAC GACAGCCTCT TCATCATGGG AAGGGGTCCA 1020
AGTGAGGGTG GGCGACTGGC TACGCCTCAG GGTGGGATCA TGGGGGGTGG GATGCAGGGC 1080
CTGAGGCAGG GAAGAACTGG GGACCAAGCC AGGCACATGT GCATATGCAT GTGCGTGCAT 1140
GTGAATATGA GTGTGTGTGT GCACCTGAGA TGGGCAGGCC CGGTTGGGAG CCCATCCACC 1200
AGCACTGCGC CCCGAGGAAG AGGAGATGCT GCTCCTACTC CAAGGTCTGA GGCTTAGGAA 1260
CCAGCTTTTG CTCTGAGTGT GACATTTCTA GGAAACCTCT GGTTTTAGCT TAAGTGTTCA 1320
CATAGGTTTT GTACCACAGA GAACCATGTG ACTTTTTTTT TTTATCCCTG ATAAGCACCA 1380
GCCTCTCCCC 1390
|
