| Tag | Content |
|---|
EnhancerAtlas ID | HS176-39329 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr8:25045150-25046340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr8:25045915-25045926 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr8:25045915-25045926 | GGATGACTCAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_02618 | chr8:25044974-25046539 | Astrocytes | | SE_04853 | chr8:25044838-25046725 | Brain_Cingulate_Gyrus | | SE_06020 | chr8:25040779-25046728 | Brain_Hippocampus_Middle | | SE_06764 | chr8:25040866-25047493 | Brain_Hippocampus_Middle_150 | | SE_09710 | chr8:25044845-25046536 | CD14 | | SE_35219 | chr8:25040444-25046458 | HeLa | | SE_36741 | chr8:25044885-25046769 | HMEC | | SE_45753 | chr8:25040706-25046911 | Osteoblasts | | SE_56329 | chr8:25044773-25047072 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCAACAGGAT AAAGTCTGAG CCTCCGTTCC AAGGTTCCTA TAATCTGGTT CAGCCTATCT 60
TCAGCATTAT CTCTCGAGGC TTCTTTCACT AGCTCTCCAA TGCAGACCAA CTGCCCTTCC 120
CACTGTTGTG CAACATACCC TGCAGAGTCC CTCCTTTGGG ACTTTGCTCC CATTGTGCCT 180
GTCCCTGCCA GGAGTGCCCT CCCAACTCTG CCTCAGACAG CTCACCTTTC CTTGAGGGCT 240
CAAATCCATT CCTACTCCCT TCTTCAAATT TGCTATTTGT CAGACTGTCC CAAACCTCCT 300
TGCTTCTTCC TCGCAGTTCC TGGACTGTGC CATCCTTGGG TTCAGTGAAT CAGACCATTG 360
TGGTTTTGTA TTCCTAGCAC TCAACAGGTG TACCAGGTAT TAGTGCATTC AGTTTGCTTG 420
TCCTTGATGT TGGGGTGCCG TTCTAAAGTA CACTAACCTA GCTTGTCTGG TAATTGAATG 480
CAGTTTTTTC CTCTTCTTTT TCTTCCCATT AGGCATAACA TCTCATTCAC CCCAATATGA 540
GTTGAATTTT GTTTGGTTAG ATGGAGGAAG GGAGAGCCTC CACTCTGTCT TTATCTCTGC 600
AAGTAAGAGA ATGAGATATT CTGCTGAGAA AACAAGGAAG CATGGAGCAG ACAGACTTTC 660
TTAAATATAG TTGGGAAAAT TGGCTTTCTG GACTTCTCTA AGTGTGTACT GGTCAGATTT 720
GGTTTCTGGA TGAAGGAACC GTAGGATAGT CATGTTGAAG CATTTGGATG ACTCAGAGCT 780
AGCTATGACT TTGCCTGTTG TGCTCTAAGA GGAGTGTGCC TCTGCAGAGC TAGTCTGTGT 840
GAGGATAGAG CTTTGGACTC AGTATGAATT GTGCCTGCTG AAGCTGGCAG TCGCTACTGT 900
CATATTTTAT CTTGGTGCCA CTCTTGGCTG TTCCTGACAT ATCCTAGATG TTTCTACAGG 960
GACTGAAATG CAGCCTGTCT GGGCTTTCTT AGTTCTTAAA CAGCAGTGTT GGCTCAGGCT 1020
CTAGCATTAA GTGGATCTCA ATGGTTTCTG TGTGTTATCA AGTGAAGTGA CTGATCTATT 1080
TGATTCTTTA AACTTATGGT GCTCTAGTAC CCCAGTGTTA AGTGCTCAGT GGCTAAGTGT 1140
TCTTCCCTGG AGACGTGGAA AATGTGCTTT TTTCTCATCT TTTTTCTTTC 1190
|
