| Tag | Content |
|---|
EnhancerAtlas ID | HS098-55618 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:101449950-101451190 |
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 | TTGACAGCAG CAGCAAGGCC AGGAAGGACC CCCCACCCAG AGCCTTCATG AGGAGCATGA 60
CCCTGCTGAC ACCTAACTTC AGACTTCTGG CCTCCAACAC AGTGAGAAAA AGAATTTCTG 120
GTGTTCGAAG CCACCCAGTT TGTGGTAGTT AGTTATGGCT GCCACATAAT GAACATATGC 180
CCAGTAAGAC CTTAAGGACC TGGAGGGCAG GACCCACGTC TGTTGTGTTC ACTGTTAAAT 240
CTCCAGTGCC TGGAGGATAA ATGGTCCTCA GCACGCCTTT GCTGAAGGAA GGTGTCTAAT 300
CCTGAGCAGG GTGACTGAAG CAAGAGGGAA GAGAGCTGAC TGAGTTGATC TGCTTAGTCC 360
CATGGAGAAA AGCAGCAGAG AAGAGGAAGA AACTGAACTT GGCTCTTCCT TCCCCATTTC 420
ACTCTCAGAT GCTGAAATGA CTATTTTTGG TGAATGCAAA TCATAGCTGT GGCCAGTGTC 480
TTCAGTCCAA GGCCACAACT GCACGCGCTG AGCCAGGGTT ATAGTCACAA GAGTTTATTT 540
TTAAAGTAAC CACGCCTGAC CTTCAGGCTC AGAGGCTGCA GACTCAGACT TTCCTGGTCA 600
GGGCCACCCC AGGGTGGCCA GTCATACTCA GCAGAGAAAA GCCACGTGTT CCAAAATGGA 660
AAAGGCGCTC AGGCTTCTTC CTCCACCACA GCTAAGGAAT ACCTTCCCCT CCCATCTGTC 720
GCCTACATGC TGACCGCTTT CTGGCGCATT TAACACCCAC AAATCACAAG CTGTTGCTCT 780
TGGCTTGGAG CTCCAGTTTC TTGAACTAAA TTATAAGTAT GAGCATGCTG TGTAGCTTGC 840
AGGGTGTGGC TGCTGGAAGA ACACTCTCCC ACGAAGGCAG AGAGCTCCCT GACCCCTTGA 900
TCATCCCCAG AAGGGACAAG AAAGCATTCT TCAGAACTGC TGGATTTTTT TTTTTTTTTT 960
TTTTGGTCTT AGTTGAGCCA TAAGTAAGCA GCAGCAGACT GTCCATAGGT ACAACATAGG 1020
TTGTCAAAGA CCAGGATTCT CTCATGTCTC AGAAGTTCTC CAGGTCCCAG CTGAAGAACA 1080
CCTTCAGATA GACGCAGTGG CTTATGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGCGG 1140
GAGGATTCCT TGGGCCCAGG AGTTCGAGAC GAGCCTAGGC AACATAACAA AACCCCATCT 1200
TTACAAAAAA TACAAACATT GACTGGGTGT TGTGTCATAT 1240
|
