| Tag | Content |
|---|
EnhancerAtlas ID | HS052-03300 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:204319590-204320820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX5 | MA0510.2 | chr1:204320203-204320219 | AGTTACCACGGCAACC | + | 6.21 | | RFX5 | MA0510.2 | chr1:204320203-204320219 | AGTTACCACGGCAACC | - | 6.28 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23313 | chr1:204319448-204321081 | Colon_Crypt_1 | | SE_24138 | chr1:204319800-204321034 | Colon_Crypt_2 | | SE_28816 | chr1:204318597-204321101 | Fetal_Intestine_Large | | SE_33663 | chr1:204319261-204321062 | H2171 | | SE_50227 | chr1:204316786-204321139 | Sigmoid_Colon | | SE_52903 | chr1:204319289-204321122 | Small_Intestine | | SE_65374 | chr1:204317203-204320948 | Pancreatic_islets |
|
| | 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 |
| GH01I204347 | chr1 | 204316837 | 204321118 |
|
Enhancer Sequence | CATCCCACCA CCATCCCCTC CGCAGGGCTG GGCTCAGAGC AGGGTTGGCC TCTAGTGCAA 60
GCTCTTCACA GGCTGGAAAG CAGCCACCAA ATCAAAAATC ACTATGGAAG GAGAGGAAGG 120
AACCCACCGC TGACGGTGCC AGGCACTGCT CCCAAACGTG TGCTCTGGAG GTCCAAGTTC 180
TCTCCATTTT ACAGATGAAG AAATCAAAGC TCAAAGAGGT AAAATTGTCT GGGAGATGGG 240
GGCGGGGGGA GGACCAGGAC TGACGTCTTG GTTTGGATGG CCCCTGGTTT TATCACTGCC 300
AGGGTTAGCT CCTGAGCCGC CCTGTCAAAT CCCCTAAACG TCCCATGAAG GCCAAGACGA 360
CTCACACTGC AAAACATACA CACAAAGGGT CGGAAACAGC ACAACATTCT TTCCTACCTG 420
CCTTTTTCTG GCTTTCCCAG TCCCACGAGG GAGAGAGGAG AGGGCTGTGC TGGGGGCATC 480
TGGGATCTGT CTTCCTCCTT GTCCAGCCCT TGTCCTTCTC TGCCTCTTTT GAGGCTGACT 540
TCCCCCAGCT CACCACCCTC CTCTCCGAAC GCCAGCTAAC CGGTTACCCG GGCAACCCAG 600
CTGGGAGGCC GCCAGTTACC ACGGCAACCC AGCATGGCCG CCAGGCTGCC TTGCTTAGGA 660
AGGTCAGGGG ACCAGCCGGG CTACCGAGCA GCTGGGATGC TGCTGGCAGG ACTGGCCCAG 720
GCAGGGGGAG TGGGGTGTGG CGGGGGGGAG GTGGCCTACG TGCCTGAGAT AACTAAGTTC 780
CTGCTGTCAG GGGCCACCTT TCCCTTTGAC ATGTTTCCCA TGAAGCAGGC TCCCCCAACT 840
TGGGCATGAA CCACAAGCCG TCCTCCCCAG TTCCATCACC CAAGCCGAAC CCGACCCCTC 900
CCACCTTCTC TACAGAGTTC CGGTCGCCTC ACCTCCAGGA AGGCTTCTCA GGCTGAGCAG 960
CAGCCAGCTG TCATTCAGCC TAACCCCAGG CCCTCTCACC CTCCGCCCTT CCTGAGCATA 1020
TCCAGGAGTC CACACATATG CAACATGCGT GTGTCAGCGT GCAGATGTGG TCTCTCTGTG 1080
AAATATGGTG GTAAAAATCA TAAGGAAGAG CTAATATTTT CTAGTACTTA CTATGTGCCT 1140
AGCATGTTGT AGGTGACTTG TGTGAAGTTT CTCAATTGAG CCATACAACA ATCATATTAT 1200
CCTCACTTCG CAGATAGAGT GCCTGAGACT 1230
|
