| Tag | Content |
|---|
EnhancerAtlas ID | HS068-05005 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr6:158985110-158986280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr6:158985349-158985360 | CCACACCCTGC | + | 6.62 | | PLAG1 | MA0163.1 | chr6:158986071-158986085 | ACCCCTTGGGCCCC | - | 6.47 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32270 | chr6:158983838-158986659 | Gastric |
|
| | 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 |
| GH06I158563 | chr6 | 158984433 | 158991432 |
|
Enhancer Sequence | GTACTTAACT CTTGAATAGC TAGAGAAATG ACTTATACCC AAGTTGGCTG ATTGAAATTT 60
TAGAGTTCCT ATCCTGCTCC CTTTGAGAAG TTTCTTTTCA AAACCCATTA GCTGGTAGGT 120
TACTTGAAAA GGAAAGATTT TAGTGAGGGG CCAAACAGTG AATGTGAGGG AGTGGTGGGC 180
CTTCTTTCTG CCCCGACCTC CACATTCTGG GTGTGCATTT GTGGGTTCCA GTCCCACCTC 240
CACACCCTGC TGCCTGGGGC CTCAGTGGGC CTGCATCCTC TCACCCCAGC CTGTGTTTTC 300
CCACCTGTGA AATGGGCCGA TGTGCCTGTC TTACAGGGAA GCTCCCAGCC TGGTACCAAA 360
TAGGTGCTCA GGAAATGCCA GCTCCCACCT CTGCGGCAGC CAGCTGGAGG GGAGACTTCA 420
TACAGTGGGG TCTTTGAAGA TGTTGTTAGA ATGAAATCCA AAATGCTTTC AAACAGAAAA 480
AGTAGAGGAG AAAAAGCACA GCCATCGTTT CTAATAGCTA GCCTGGCTGA GTTCTTGCCA 540
CGCTGTTCTG ACCACTATGT TTATGATTCC ACCCGCACCT GCCAGCAACT CTGTGAGATG 600
AATCTTCTGC CTCTCTCCAT TTTGCAGATG AGGAAACTGA GGGTCTGGGG AACTGTTTAC 660
TTGCCTGCTG TCATGTGGTC AGGAAGTGGG GAGCCAGGCT GTCAGGCAAC AGGCCGGCAT 720
TTTGGGCCAA AGGAGAAGAG ATTATTTTTA TACAGATTGG AAAAATAAAA ACAACAGTGT 780
GAGAATGGGC TGGGAGATTT AAAGTCCCCG ACTACTGCTC AGATCCTAAT TTGTCAATTC 840
TCATGTGGGA GATGCCGGCA TGAGTTGAAC AAGCAGCAGG ATGTGTAGTA CCAGAAGTTC 900
TCGGTCTTAC CCGCCTACCG TCGTGGTGGT TTGCGGAGAC CGAGATGAAG GTGTCTCTCA 960
CACCCCTTGG GCCCCTGCTG CGGATGCTGG TGTTGCTGGG TTCTGTAGAA GTGGGAATGC 1020
TGGTGCTGGC TTCCCTCACA TCTCTGTCCC TCTCGCTGCA GGACAGCAAT TTGAGGTGTT 1080
CTCACGACCT CTGCTTACCC GGATTGTATC TGTTTTGTGG TTCTGTGCAG CAGTCCTAGG 1140
GCAGCTGAGT GCTTGCGGAC TGCTCGCCTC 1170
|
