| Tag | Content |
|---|
EnhancerAtlas ID | HS180-24494 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr19:41921780-41922940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23546 | chr19:41922567-41923038 | Colon_Crypt_1 | | SE_27542 | chr19:41921691-41923047 | Esophagus | | SE_65911 | chr19:41918946-41923155 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 41922115 | 41922580 | | chr19 | 41921900 | 41922020 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I041415 | chr19 | 41921858 | 41922993 |
|
Enhancer Sequence | TGACCTTGCG ATCCGCCCTC CTCCACCTCC TAAAGTGCTG GGATTACAGG CGTGAGCCAC 60
CATGCCTGGC CTTTTTTTTT TTTTTTGAGG TGGAGTCTCA CTCTGTCGCC CAGGCTGGAG 120
TACGGTGGCG CAGTCTTGGC TCATTGCAAC TTCTGCCTTC CAGGTTCAGG TGATTCTCCT 180
GCCTCAGACT CCGGAGTAGC TGGAATTAAA GGCATGCACC ACCATGCCTG GCTAATTTTT 240
GTATTTTTAG TAGAGATGGG GTTTCACCAC GTTGGTCAGG CTGGTTTCAA ACTCCTGACC 300
TCAAGTGATT CGTTTGCCTT GGCCTCCCAA AGTGCTGGGG ATTACAGGCA TGAGCCACCG 360
CGCCGGGCCA GCCAAGGTGC TGTTATATGT GCTCTTTAGC CTCGGAGACT GTCATTTCCC 420
CTCACTGCAC TGCAGAGCGA GGGCACACCG GGTGAGGTTA GGGCAGGCCC CAGTGGTGTT 480
GCCTCATTGA GGCACCTCCC CCATCCATGT GAGGCAGGAG AGGCAAGCAT TACCATCAAC 540
TCTAAAAGCC AGGTAAGAAC CTGAGTCAAC AAAGGTGAGG TCATGGGCCC AGGCCACATT 600
CTCCTAAGGA GTGGAGCCGA GTCTTTTTAT GGCAGTCTGA CCCAGAGACA GCTCTCGCTG 660
TTTCCCACCC TTGGCTGTCT TCCCAGGGCT ATATGTGGAG TATCAGTGGT GGCACTGGCA 720
GGGAGTGGCG CCCGGTGAAA AGGAGTGTTA AGAGGAAGCA CGTGCCAGGT GTGGTGGCTC 780
ACGCCTGTAA TCCCAGCACT TCGGGAGGCT GAGGCGGGAG GATTGCTTGA GCCCAGGAGT 840
TTGATACCAG CCTGGGCAAC ATGGCGAGAC CCCCATCTCT AAAAAATTAA AAAATTAGCC 900
AGGCGTGGTG GTGCACACCT GTAGTCCCAG CTACTCAGGA AGCTGAGTGG GAGGATTGCT 960
TGAGCCCAGA GGTTCAAGAC TGCAGTGAGC TATGATTCCA CCACCGAACT CCAGTTTGGG 1020
TGACAGAGTA AGATCCTGTC TCTGAGACCA ACAAGAAAAG AGGTAGCATG TGTCAAGCAA 1080
GAGCAGCAGT TCCCACTGGA CCTGGAGTTT CCTGGTGCAA ATCAGCCTGT GAGTCTGTAT 1140
TTTCTTTTTT CTTCAAGACG 1160
|
