| Tag | Content |
|---|
EnhancerAtlas ID | HS007-01252 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:204319160-204320390 |
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 | ACATTCTGGC CAGGCGCAGT GGTTCATGTC TGTAATCCCA GCACTTTGGG AAGCTGAGGC 60
AGATGGCTCA CTTGAGCCCA GAAGTTCAAG ACCAGCCTGG ACAACATGGT GAAACCGTCT 120
CTACCAAAAA ATACAAAAAT TAGCTGGGCA CAGTGGCAAG CACGTGTAGT CCCAGCTCCT 180
TGGGAGGCTG AGGTGGGAGG ATGGCTTGAG CCAGGGAGGT CAAGGCTGCA ATGAGCTATG 240
ATGTCACCAG GACACTCCAG CATGGGTGAC AGAGTAAGAC CGTGTCTCAA AAACAAAAAC 300
AAAAATAAAA AAACCTTTCT TGCTCTTGCA GATGTTCCAA CCTGTGTAAC TTGTGTTCTG 360
CCCTCAGCAG AGTGAGCTGG TAAACTCCTT GAGGTAAGAG CCATGTCTCT AATTTGTCAA 420
GAATTCCAAC CATCCCACCA CCATCCCCTC CGCAGGGCTG GGCTCAGAGC AGGGTTGGCC 480
TCTAGTGCAA GCTCTTCACA GGCTGGAAAG CAGCCACCAA ATCAAAAATC ACTATGGAAG 540
GAGAGGAAGG AACCCACCGC TGACGGTGCC AGGCACTGCT CCCAAACGTG TGCTCTGGAG 600
GTCCAAGTTC TCTCCATTTT ACAGATGAAG AAATCAAAGC TCAAAGAGGT AAAATTGTCT 660
GGGAGATGGG GGCGGGGGGA GGACCAGGAC TGACGTCTTG GTTTGGATGG CCCCTGGTTT 720
TATCACTGCC AGGGTTAGCT CCTGAGCCGC CCTGTCAAAT CCCCTAAACG TCCCATGAAG 780
GCCAAGACGA CTCACACTGC AAAACATACA CACAAAGGGT CGGAAACAGC ACAACATTCT 840
TTCCTACCTG CCTTTTTCTG GCTTTCCCAG TCCCACGAGG GAGAGAGGAG AGGGCTGTGC 900
TGGGGGCATC TGGGATCTGT CTTCCTCCTT GTCCAGCCCT TGTCCTTCTC TGCCTCTTTT 960
GAGGCTGACT TCCCCCAGCT CACCACCCTC CTCTCCGAAC GCCAGCTAAC CGGTTACCCG 1020
GGCAACCCAG CTGGGAGGCC GCCAGTTACC ACGGCAACCC AGCATGGCCG CCAGGCTGCC 1080
TTGCTTAGGA AGGTCAGGGG ACCAGCCGGG CTACCGAGCA GCTGGGATGC TGCTGGCAGG 1140
ACTGGCCCAG GCAGGGGGAG TGGGGTGTGG CGGGGGGGAG GTGGCCTACG TGCCTGAGAT 1200
AACTAAGTTC CTGCTGTCAG GGGCCACCTT 1230
|
