| Tag | Content |
|---|
EnhancerAtlas ID | HS012-14596 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr17:40693220-40694100 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_24066 | chr17:40692725-40693505 | Colon_Crypt_2 | | SE_24066 | chr17:40693510-40694022 | Colon_Crypt_2 | | SE_25138 | chr17:40692712-40694055 | Colon_Crypt_3 | | SE_28881 | chr17:40692606-40694128 | Fetal_Intestine_Large | | SE_35596 | chr17:40692565-40694399 | HepG2 | | SE_57057 | chr17:40692969-40693927 | VACO_400 |
|
| | 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 |
| GH17I042540 | chr17 | 40692702 | 40698177 |
|
Enhancer Sequence | GCAGGTACAG TGCCTGGGTG GGGTGGGAGA GCCCCCCAGA CCCTCAAAAA GAAGGGAGTA 60
GCAGATGTCA GTAGGGGTAG GCAGAGGGAC TGGAATAATG CCTCGCCATA ACACACAGTA 120
CTTCATAGTT TACCAAGCAC GTGTACACAT GCGTTGTCTC AGTGAATCCC ACTGTGGTTG 180
AGAGGTGAGC TCTGGAAGCC AACAACCTGG GTCACACCTC GCGCTCCTAT TTCCTGGCCG 240
TGTGACTTAT GACTCATGAC CTCCTTCCCA GTGTCTCGTT TGCTTTTCCT GTAAACTGGG 300
ACTACCTCAT AGGTAGAATA ACGCCTGGCC CAGAGCAAAG GCCACTAAGA GCTAGCTATG 360
AACAAGGATT TTGTTTCATC TCTGCGTGGT TGCTGAAGTA GGCACTGCAG GCAGGAGGTG 420
AGTGGATGTG CCTAAAGGCA CTAAGTGCGC ATCCTGCTAC AAAACTGTGA AGCCAGGGCT 480
CCTTCCTGCC ACTTAAAGGA GGAGTGGAGC AGAGGGCGCC CAAGTCAGGA ATGACTTAGT 540
GGAGAGGCGT CTGTGTTGGC CAGGAAGGGA ACAGATCAGC TCAGCCTTTC TTGAGCAGTA 600
CTGCTCCAAG TGTGACCCAA AACCAGCAGC AGCAGCAGCA GCAGCCCGAG CTGTGAGATG 660
GCAAATTCTC AGGCCCTACC CAAGACCTGA AGGAGAAGCT ACATTTTTTT TTTTTTTGAG 720
ACAGATTTCA CTCTGTTGCT GAGGCTGGAG CACAGTGGCA CAATCTCATC TCACTGCAAC 780
CTTCGTCTCC TAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTATA 840
GGCACCCGCC ACCACGCCCG GCAATTTTTG TTTGTTTTGA 880
|
