| Tag | Content |
|---|
EnhancerAtlas ID | HS109-22329 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr8:101449840-101451010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr8:101450788-101450799 | GCAGGGTGTGG | - | 6.62 | | Klf1 | MA0493.1 | chr8:101450790-101450801 | AGGGTGTGGCT | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27991 | chr8:101449856-101452919 | Fetal_Intestine | | SE_28830 | chr8:101449753-101453025 | Fetal_Intestine_Large | | SE_32533 | chr8:101448020-101453094 | GM12878 | | SE_62291 | chr8:101421434-101542088 | Tonsil |
|
| | 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 |
| GH08I100437 | chr8 | 101449399 | 101453077 |
|
Enhancer Sequence | AGAAGAAAAG AAAGATGTGG ACACAGAAAC CTAGACACAC AGGGCAGAAG CCATGTGAAG 60
ACAGAGGCAA AGACTGGGAT GAGGCAGCAA TAAGCCAAGG AAGGCCGAGG TTGACAGCAG 120
CAGCAAGGCC AGGAAGGACC CCCCACCCAG AGCCTTCATG AGGAGCATGA CCCTGCTGAC 180
ACCTAACTTC AGACTTCTGG CCTCCAACAC AGTGAGAAAA AGAATTTCTG GTGTTCGAAG 240
CCACCCAGTT TGTGGTAGTT AGTTATGGCT GCCACATAAT GAACATATGC CCAGTAAGAC 300
CTTAAGGACC TGGAGGGCAG GACCCACGTC TGTTGTGTTC ACTGTTAAAT CTCCAGTGCC 360
TGGAGGATAA ATGGTCCTCA GCACGCCTTT GCTGAAGGAA GGTGTCTAAT CCTGAGCAGG 420
GTGACTGAAG CAAGAGGGAA GAGAGCTGAC TGAGTTGATC TGCTTAGTCC CATGGAGAAA 480
AGCAGCAGAG AAGAGGAAGA AACTGAACTT GGCTCTTCCT TCCCCATTTC ACTCTCAGAT 540
GCTGAAATGA CTATTTTTGG TGAATGCAAA TCATAGCTGT GGCCAGTGTC TTCAGTCCAA 600
GGCCACAACT GCACGCGCTG AGCCAGGGTT ATAGTCACAA GAGTTTATTT TTAAAGTAAC 660
CACGCCTGAC CTTCAGGCTC AGAGGCTGCA GACTCAGACT TTCCTGGTCA GGGCCACCCC 720
AGGGTGGCCA GTCATACTCA GCAGAGAAAA GCCACGTGTT CCAAAATGGA AAAGGCGCTC 780
AGGCTTCTTC CTCCACCACA GCTAAGGAAT ACCTTCCCCT CCCATCTGTC GCCTACATGC 840
TGACCGCTTT CTGGCGCATT TAACACCCAC AAATCACAAG CTGTTGCTCT TGGCTTGGAG 900
CTCCAGTTTC TTGAACTAAA TTATAAGTAT GAGCATGCTG TGTAGCTTGC AGGGTGTGGC 960
TGCTGGAAGA ACACTCTCCC ACGAAGGCAG AGAGCTCCCT GACCCCTTGA TCATCCCCAG 1020
AAGGGACAAG AAAGCATTCT TCAGAACTGC TGGATTTTTT TTTTTTTTTT TTTTGGTCTT 1080
AGTTGAGCCA TAAGTAAGCA GCAGCAGACT GTCCATAGGT ACAACATAGG TTGTCAAAGA 1140
CCAGGATTCT CTCATGTCTC AGAAGTTCTC 1170
|
