| Tag | Content |
|---|
EnhancerAtlas ID | HS060-33870 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr8:101449910-101450810 |
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 | AGACTGGGAT GAGGCAGCAA TAAGCCAAGG AAGGCCGAGG TTGACAGCAG CAGCAAGGCC 60
AGGAAGGACC CCCCACCCAG AGCCTTCATG AGGAGCATGA CCCTGCTGAC ACCTAACTTC 120
AGACTTCTGG CCTCCAACAC AGTGAGAAAA AGAATTTCTG GTGTTCGAAG CCACCCAGTT 180
TGTGGTAGTT AGTTATGGCT GCCACATAAT GAACATATGC CCAGTAAGAC CTTAAGGACC 240
TGGAGGGCAG GACCCACGTC TGTTGTGTTC ACTGTTAAAT CTCCAGTGCC TGGAGGATAA 300
ATGGTCCTCA GCACGCCTTT GCTGAAGGAA GGTGTCTAAT CCTGAGCAGG GTGACTGAAG 360
CAAGAGGGAA GAGAGCTGAC TGAGTTGATC TGCTTAGTCC CATGGAGAAA AGCAGCAGAG 420
AAGAGGAAGA AACTGAACTT GGCTCTTCCT TCCCCATTTC ACTCTCAGAT GCTGAAATGA 480
CTATTTTTGG TGAATGCAAA TCATAGCTGT GGCCAGTGTC TTCAGTCCAA GGCCACAACT 540
GCACGCGCTG AGCCAGGGTT ATAGTCACAA GAGTTTATTT TTAAAGTAAC CACGCCTGAC 600
CTTCAGGCTC AGAGGCTGCA GACTCAGACT TTCCTGGTCA GGGCCACCCC AGGGTGGCCA 660
GTCATACTCA GCAGAGAAAA GCCACGTGTT CCAAAATGGA AAAGGCGCTC AGGCTTCTTC 720
CTCCACCACA GCTAAGGAAT ACCTTCCCCT CCCATCTGTC GCCTACATGC TGACCGCTTT 780
CTGGCGCATT TAACACCCAC AAATCACAAG CTGTTGCTCT TGGCTTGGAG CTCCAGTTTC 840
TTGAACTAAA TTATAAGTAT GAGCATGCTG TGTAGCTTGC AGGGTGTGGC TGCTGGAAGA 900
|
