| Tag | Content |
|---|
EnhancerAtlas ID | HS176-00464 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:27175480-27176290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:27175994-27176005 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr1:27175994-27176005 | GGGTGACTCAG | + | 6.02 | | ZBTB18 | MA0698.1 | chr1:27175584-27175597 | ATTCCAGATGTGT | + | 6.02 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_23384 | chr1:27174699-27178454 | Colon_Crypt_1 | | SE_24351 | chr1:27174710-27177316 | Colon_Crypt_2 | | SE_26621 | chr1:27173970-27186608 | Esophagus | | SE_34025 | chr1:27175414-27176113 | HCC1954 | | SE_34526 | chr1:27174651-27176664 | HCT-116 | | SE_50491 | chr1:27174691-27177388 | Sigmoid_Colon | | SE_53016 | chr1:27174654-27177272 | Small_Intestine | | SE_57686 | chr1:27174839-27175963 | VACO_503 | | SE_57686 | chr1:27176013-27177166 | VACO_503 | | SE_64263 | chr1:27174693-27178982 | 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 |
| GH01I026847 | chr1 | 27174110 | 27178056 |
|
Enhancer Sequence | GCTCTGAGGT GTGGGGCAGA CAGACAGGCT TTGAACCCTT CTCCCAGGCT TCAGCCCGGT 60
CCTCAAGAGG TCCAAGCTCC CAGGAAACAG ACTGGAACAA TAACATTCCA GATGTGTTTG 120
GGCCAGAAAG AATGAGTTAC TGTCCAGTGG CCCAGGGCCA GCTGTACTGA AAAACTTTGA 180
TCTGATTCCC AGAGTTGAGA GGGAAAAGCA TCTAGCAACA GAGGCGTTTA AGCTGATGAG 240
GTGCAGAGGA TGTCACCACT GGAAATGGCT CCTGACCCTA CAGCTGCCTG CAGTGGTTGT 300
TTTGTCCCCT CTCCCTGCTC TCCAGAGGCT GTGTAGTTCT GATGGGCACC CTGAGAGGGT 360
GTTGTAAGGG AAATAATGCA TGAGAGGGCC CAGGTGAGCT GAGCCACAGT GACTGTGCAT 420
AGTTCCCAGG GCAGTGAGCT CATCATGCCA GCTCAGTACT CCCTAAGCAA GAGAACAGCA 480
GGGAACACCC CCCCGTGACG GCATGCAGTG AAGGGGGTGA CTCAGTGGGC ACCATTCATC 540
CCCAAGGAGC TGCCCCGCCC ACGCCGTGCA AAGGGCACTG GCCTTGGCAT GAGGCCTGCA 600
ATGGGCTTGT GACCCACATT CCCACAAGGA CTTTCTTTAC CAGTCTGGGT GTGCCTCCAC 660
CCCCGGGGAC AGTGTGCAGG TGAGCTCAGC CCTTTGACCT GGCCTGTGAT GCTGGCTGGC 720
TGTGAACCCC ATTGCAGCTC AGCCCCTCCC TGGGCCGCTA GTCCTAGAGC AGGAGACGGG 780
TTGTTGACTG TTAGCATGTG GTTGGGATGG 810
|
