| Tag | Content |
|---|
EnhancerAtlas ID | HS050-40685 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:239552630-239554120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_44462 | chr2:239551172-239556139 | NHDF-Ad |
|
| | 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 |
| GH02I238642 | chr2 | 239551444 | 239554673 |
|
Enhancer Sequence | AGTGCAGGGT GGGAAGAGAC CTGGGAAGGA GGCTTTGGTC CAGGTCCTAG AGCAGGCTCC 60
AGTGTGACTC CAGGAGACTG AGATATCCAG GGGCCATCCC ACACTGTGCT TCCTAAAGTC 120
TACTTAGCGG CCCCCTCACT CACTGGATAA GAACAGTGGC TTCCTCCTCA CTGAGCTTTC 180
ACTGGTGCCT TAGGCTCCAC TGTTGGAGAT CTAGTTGTTT TAGTCACTCT GTTGTCTCAT 240
GCTGGAGAGA AGCGACCTTT CACATGAGAG TTAGTCACTT GTCTATGGTG AGTCAGATGC 300
TATCAGCTGC CCTTGGTGAC AGGAGGCTAT GGATGGATAT TAATGGCTGG GAGGAGGGTC 360
AGGAGGCCAC CAGCAAGCTG AAAAGAGTGG CTTGGAGAGG TGACAGTAAG TCCTAGAAGG 420
AGAGATGAGC CTGGGAATGT CCAACTCCAT CGGCTGACAG GGCTGACCTG CTCTGCACCT 480
GCCGTGTGAA AGGTACCTGG GTCTGAGTCA GGTCCCGTAG GGCCCAAGCA CACTCACATG 540
GACTTCCTGT TACTGGGGCT GCAAAGAGTT GCTACTTCCA ACTGGAAGGG GCTCTGACCA 600
AATTCACAGC CCTGGACCAA TCTTTCTGTT TGGCTTGTAG CAAACTTGCA AATTCCTGTG 660
AGGGGAAACA AGATTTATTT CTCATTGAAA CATTCACAGA AGAATCAGGT TCAAATAATT 720
ATTCCCGACT TCACTTCCCT TTTACTCTGC GTTGCTTCAC AAAGACGCAC ACACACGCAC 780
ACAGAAATGA GTCATATGTT CAGCTTTCTG AAAGTCAAAG AGAATAAACA GATGCCACAG 840
AGGAGATGGA AAACTGGCAT TGTTTTAATA AAAACTCTGA AGACAAAGGA AGGAACAGAA 900
ACTTAAAGAT TTAAAAGAGC AAATCCCAAT GGTGGGTGAT TCAAACATCT TTCCAATTCC 960
CACTCCCACC CCAGGAAATG CTCCCTAAGC GTGAAGGAGG GAGGTGTCTG CAAGCTTCCT 1020
GCTGACATGG CCCGGGACAG GCAGAGTCCA AGAACAAAGG ACTGGCTAAG AAAAGCATGG 1080
AGATCAAAAA TACTTAAAAA TATACATGGG TATGAAAAGG GTTAGACAGC TAGAAAACAA 1140
AATACAAAAT GTCACCTTTG AGTAGTGAAG TTTTGGATGA TTTTTATTTT CTTATTTTAT 1200
ATAAAATTTA TAACAGGGGT CCCCAATCCC TGGGCCATGG ACTGGCACTG GTACCTGTCT 1260
GTGGCCTGTT AGGAACCAGG CCTCACCGGG CCTCACGGCA GGAAGTGAGT ATTGGGTAAG 1320
CGAGCAAAGC TTCATCTGTA TTTACAGCTA CTTCCCATCA CTCACATTCT CACCTGAGCT 1380
CTACCTCCTG TCAGATCAGC CGCAGCATTA GCTTCTCGTA GGAGCACAAA CCCTACTGTG 1440
AACTGCGCAT GTGAAGGATC TAGGTGTGTA CTCCTTACAA GAATCTAATG 1490
|
