| Tag | Content |
|---|
EnhancerAtlas ID | HS108-34681 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:41504380-41505690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK4 | MA0076.2 | chr6:41504877-41504888 | GCCGGAAGTGC | - | 6.14 | | TCF3 | MA0522.2 | chr6:41504809-41504819 | AACACCTGCT | + | 6.02 | | TFAP2A | MA0003.3 | chr6:41504822-41504833 | TGCCTGAGGCT | - | 6.32 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27953 | chr6:41503923-41507175 | Fetal_Intestine | | SE_28956 | chr6:41503802-41507213 | Fetal_Intestine_Large | | SE_31492 | chr6:41503924-41506100 | Gastric | | SE_65317 | chr6:41504216-41505554 | Pancreatic_islets |
|
| | 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 |
| GH06I041536 | chr6 | 41503971 | 41507010 |
|
Enhancer Sequence | GATTCTAGTT TCTAGAGTGA CTGGGTAGAT TATGGTGCCA CCAATGGGGA GAAAATGCAG 60
AGGTGGAGCA TGTTATGGAT ACAGAAGATG GCTTGGGCTG GGGACATGTT GAGTGTGCCA 120
TCCCTGGAGG CCCACAAACA CGCACATGGG ATCCAGGTCC CACACAGGAT AGTAGTGGGA 180
GCCACCATCT CAAAAGTGGA AGGTAAAACC ATGAGAGTAG ATGGGCTTGT CCGAGAGCAC 240
AGATGACGAG GACAGAGTGG GGCAACGCCC AGTGCTTCAG ACAGGACAGA GGGAGATGAG 300
ATGAGCCCAC AAAGACTCAT GAAAAGGAAA AGTTAAGCAG GAGAACAGAC CGGCAGAGTG 360
TGGCAGGCAC TGGCGCCCTG CCCATCTCTC TCAGTGTTCG CCTCTAAAGG TAGAAGCCTG 420
CTTACTGCCA ACACCTGCTG TTTGCCTGAG GCTTTTTTCC TGGCCGTGGA AACACCCTTG 480
GCTCCAGCCC AGAGCAGGCC GGAAGTGCTG GAGAGTGAAT GCGCCTAGAA GGAGGACGCA 540
GCCCACGATG AAGGGGAAGT TGGTGGATGA GTACCCTAAG GCCTGCGTCC GTGGGCTGGC 600
TTGTGTGCGG TGTGTGTTAC GCACGCTCAA GTCCTCAGTG GGACTGCACT CCTCTTGCTG 660
ACAGTGGGAT AACACTCCCT TTATTGGCTG CCTTCCCTTC ATTCTCCCTG CCCTGCTCCC 720
CCACTGGTAT TTCTGGGACC ACCTCCCAAA TAAACCACTT ATGCTTGAAT CACTGTCAGA 780
GTCTGCTTCA GGGAGAACCT AAACTAAGAC AAACATGTCA TGAAAACCAA ACAAATAGAA 840
AACATGAAGG TGTTCTCACC AGGTAACTTT TGTCTCTGGA GGGATCAGGT CTTTCCTGTC 900
CCAAGGGGCC CACCTCCACT CTCATAAAAG AGGCCAATTT CTTGTCTGGT CCGAAGGTTC 960
TCAGCAGGGG ACTTTCCACA TTCCCTGGCT GAGCAAACTC TAACATCAAG AAATCCTTTT 1020
GTAGTCCCAG CTACTCAGAG GCTAAGGCAG GAGGATCTCT TGAGCCCAGG AATTCAAGGC 1080
TGCAGCGAGC TATGGTCATG TCACTGCACT CTAGCCTGGG TGTCAAAGTG AGATCCTGAC 1140
TCTAAAATAA GACAGAAAAA AATAAATACT TTCCTGTCTC TCATCTCATT CCTTCTGTTT 1200
TTGCAGGAGC TGCTGTGTAC TGCAAATGCT CAGAAAGATT CCTCAGCCCC GAGCCCGCCC 1260
TCGCCTTGTA CCCCTGATTC AGTACTCTTC TTTTCCAGCA CTCCAGGTGG 1310
|
