| Tag | Content |
|---|
EnhancerAtlas ID | HS051-02102 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:204319680-204320930 |
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 | ATCAAAAATC ACTATGGAAG GAGAGGAAGG AACCCACCGC TGACGGTGCC AGGCACTGCT 60
CCCAAACGTG TGCTCTGGAG GTCCAAGTTC TCTCCATTTT ACAGATGAAG AAATCAAAGC 120
TCAAAGAGGT AAAATTGTCT GGGAGATGGG GGCGGGGGGA GGACCAGGAC TGACGTCTTG 180
GTTTGGATGG CCCCTGGTTT TATCACTGCC AGGGTTAGCT CCTGAGCCGC CCTGTCAAAT 240
CCCCTAAACG TCCCATGAAG GCCAAGACGA CTCACACTGC AAAACATACA CACAAAGGGT 300
CGGAAACAGC ACAACATTCT TTCCTACCTG CCTTTTTCTG GCTTTCCCAG TCCCACGAGG 360
GAGAGAGGAG AGGGCTGTGC TGGGGGCATC TGGGATCTGT CTTCCTCCTT GTCCAGCCCT 420
TGTCCTTCTC TGCCTCTTTT GAGGCTGACT TCCCCCAGCT CACCACCCTC CTCTCCGAAC 480
GCCAGCTAAC CGGTTACCCG GGCAACCCAG CTGGGAGGCC GCCAGTTACC ACGGCAACCC 540
AGCATGGCCG CCAGGCTGCC TTGCTTAGGA AGGTCAGGGG ACCAGCCGGG CTACCGAGCA 600
GCTGGGATGC TGCTGGCAGG ACTGGCCCAG GCAGGGGGAG TGGGGTGTGG CGGGGGGGAG 660
GTGGCCTACG TGCCTGAGAT AACTAAGTTC CTGCTGTCAG GGGCCACCTT TCCCTTTGAC 720
ATGTTTCCCA TGAAGCAGGC TCCCCCAACT TGGGCATGAA CCACAAGCCG TCCTCCCCAG 780
TTCCATCACC CAAGCCGAAC CCGACCCCTC CCACCTTCTC TACAGAGTTC CGGTCGCCTC 840
ACCTCCAGGA AGGCTTCTCA GGCTGAGCAG CAGCCAGCTG TCATTCAGCC TAACCCCAGG 900
CCCTCTCACC CTCCGCCCTT CCTGAGCATA TCCAGGAGTC CACACATATG CAACATGCGT 960
GTGTCAGCGT GCAGATGTGG TCTCTCTGTG AAATATGGTG GTAAAAATCA TAAGGAAGAG 1020
CTAATATTTT CTAGTACTTA CTATGTGCCT AGCATGTTGT AGGTGACTTG TGTGAAGTTT 1080
CTCAATTGAG CCATACAACA ATCATATTAT CCTCACTTCG CAGATAGAGT GCCTGAGACT 1140
TAGAGAAGGT GAGGGACTTA CTCAAGGCTG CACAGGTACT AACCAGCAGA GACAGGGTGA 1200
GGCTGTGTAG GGACCAGCTT CCTGGAATTC CTTCAGCTCC TGCCCTCCCC 1250
|
