| Tag | Content |
|---|
EnhancerAtlas ID | HS148-09765 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr2:108883590-108885000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28382 | chr2:108881862-108885267 | Fetal_Intestine | | SE_29368 | chr2:108881814-108885000 | Fetal_Intestine_Large | | SE_55938 | chr2:108880568-108889674 | u87 | | SE_67729 | chr2:108880568-108889674 | u87 |
|
| | 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 |
| GH02I108265 | chr2 | 108882067 | 108885320 |
|
Enhancer Sequence | TTTAGGGTGA GAATTACAAG AGTCAGAAAA ATCACATCAT TCAACAATCT TGCTTTTCAG 60
ATGAGAACAC TAAGAGCCAG GGAGAGAGGG ATGGCCCCCA CAAACAGGTC ACGCAGACAC 120
GGTTCATCAG GATCCCCCGG CCCCTGGCTA GCTCCCCACA CACTGCAGGA GTCACGCAGA 180
TTGCGAAAGT CTTCTCTGCA GACTTCATCT TGCACTACTC ACTTCCTCTT AGCACTTGGA 240
ACAGCTTGGG TGTTCTATGG ATTCTCTCTG ATTACATAAG AAATTCCAAA ATTTTTCTAA 300
TGGCCTATTT AGAAAAAGAA AAACAACAAA GCCTGATGGG AATCCACTTA GAAAGGCAGC 360
TCTTCCCAGA GAGGGTCTCT GCATTAGAGC GTCTTGGAGA TGTCTGTGAG CAGGAGGGAG 420
CCCACAGCAG AAACTGCCCT TCCCCAAAGC TGAGTAAAGC CCAGCTCTGC CCTCCAGCCC 480
CATCACAAGG CTTCTGGGAT TTCTTTGGCC TGTAGGTACC AGGCTGACAC CCCCTGCATC 540
CTGCCCGACC TCATCACATC TCCCACAGGG CCTGCCCTAA GTGGAGTGGA CCGAGCTCCC 600
TATGCAGCCC CAAAGACTGT GTTCCACTGC CCTTTTCCTC ATTTTACCCC TAATAATCTA 660
GTGTGGGTTT TGCTGTTAAG GGAACTCCAA AACATCTGAG GCAAGTTTTA GTCCATATAA 720
ACTCAAGTAT GGGGAATGCC AGGAAACAAA TGACAGAGAG GAGGGTTAGG GACTGGAATG 780
AAAATCCTTA ACCCTTTCTA GGTGTTGTTA AAATGATCAC CTGGGAGGCC ATCAGACCTT 840
AGTGCCTCCA GTGTCCCAGA TTCCTATGGA AGCAAACCAA GACCCAACTC AGTTACACTG 900
AGGACTCAAC CAGTCAGAAA CCACCAATCA ACCCTGGACT AGGGACTTTC CAATTATTGC 960
TCCACTTTGA CCAATTAAAC ATTTCCCCTA TCCTGCTTCC CATTCACTCT ATAAAAGTCT 1020
CCCCACACGC TCCTTCAAAG GAGCCCTGAA TCTTTCTGGC TTGGAGCGCC AGATTCATGA 1080
ATCATTGCCT GCTCAAATAA ACTCTTTAAA ATGTTAACGT GTCAGAGTTT ACCTCTTAAC 1140
AGTTCCTATT CTATTTTTTT CAGCTTGGTA GAATTAGAGT TCATACTACA GGAATCTAAC 1200
GATCAGTCTT CTCCAAAGAG GTTTTTCAAC AGTGGAGGAC CCTCCCAGCC CTTCTCCATT 1260
ATCAGTGCCC TTTCTCTCTC CACATTCATG GGTTGTTGGT CTAGGCTCAA AGAGGTTGGT 1320
CTAGGCCACA GAGGTGGCCT GTGGGCCAAA AAATCCAGCC ATTTAGTATG GCTGGGAGCT 1380
ATGAATAAAC TGTTTGTATA CTTTTAAACA 1410
|
