| Tag | Content |
|---|
EnhancerAtlas ID | HS052-36444 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr8:22215610-22216670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr8:22216460-22216473 | TTCTGGAATTTTC | + | 6.17 | | NFAT5 | MA0606.1 | chr8:22216467-22216477 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr8:22216467-22216477 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr8:22216467-22216477 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27913 | chr8:22213499-22219154 | Fetal_Intestine | | SE_28765 | chr8:22213432-22219188 | Fetal_Intestine_Large | | SE_35465 | chr8:22212280-22219140 | HepG2 | | SE_46047 | chr8:22213577-22217586 | Osteoblasts | | SE_55927 | chr8:22213456-22217476 | u87 | | SE_67558 | chr8:22213456-22217476 | u87 |
|
| | 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 |
| GH08I022355 | chr8 | 22212607 | 22218992 |
|
Enhancer Sequence | GAGGAGTGGA ATTGGAATGT TCCTAACACA AAGAAATGAT AAATGAGCCG GGTGCCGTGG 60
CTCACACCTA TAATCCCAGC ACTTTGGGAG GCTGAGGTAG GTGGATCATT TGAGCTCAGG 120
ACTTCAAGAC CAGCTGGGCA ACATGGGAAG ACCTTGACTC TACAAAATAT AAAAATCGGC 180
CAGGCTTGGT GGTGTGTGCC TATAGTCCCA GCTACTCAGG AGACTAAAGC AGGAGGATTG 240
CTTGAACCCA GGAGGCAGAG GTTGCAGTGA GCCGAGATTG TGCCAACTCA CTCCAGCCTG 300
GGTGACAGAG CAAGATTCTG TCTCAAAAAA AAAAAAAAGA TAAATGTTTG AAGTGATAGC 360
CCAGTTACCC TGATTTGATT CTTACACATC ATATGCTTGT ATCAGAATAT CACATGTATA 420
CTATAAATAT GTACCACTAC TATGTATCCA AAAAATTAAA AATAAAATTT TAAGTACCTT 480
CCCAAAGCAC CTAGCTGCTC ACTTAAGCAC TGCATTTCTT TAGAATACTA CAGTTTCCCT 540
ATTTATTTAG AAACTCTGTG CTTCCTGAAC TCATTCTAGA AAGAACCTCA TTTCTGTGCA 600
GTAGTCTCTT ATCCATGGGG AATACATTTG AATACCCCCA GCAGTTGCCT GAAACCTCAG 660
ATAGTACTGA ATCCTATACG GTACTATGTT ATTTGAATCT GAAACTCAGG ATGTCTATTA 720
AGTGACTAAT GTGTAGCATC ACCGGTGTGG ATACTCTGGA CAGACATGAT TCATGTTCAC 780
GGGGGATGGA GTGGGACAAC GTGAAGTTTC ATCACACTAC TCAGAACAGT TTGCAATTTA 840
TAACATGAAT TTCTGGAATT TTCCATTTAA TAGTTTTGGA CTTTGGCTGA CCAAGGGCAA 900
CTGAAACCTC AGAAAATGAA ACCATGGAAA GGAGGGACTG CTGTACGGTG TGACAGGGTC 960
CTTTTTACTT GGGCAGCATT TTGTTGAATG ATGTGAAAAA GGAATTTTAG AAATGACTAT 1020
ATATTTTAAA ACCTTAAAAT TTGGGCCTGA AATTAATTTC 1060
|
