| Tag | Content |
|---|
EnhancerAtlas ID | HS184-10853 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:105346850-105349060 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_24889 | chr14:105347880-105350475 | Colon_Crypt_3 |
|
| | 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 |
| GH14I104882 | chr14 | 105348701 | 105348970 |
|
Enhancer Sequence | TCTGCATGCA TATACCATGT ACACCCATAC CCCTCACCCT TTGCACACAC CTACCCTTGC 60
ACATGCACAC CCCTCACCCA TTGTGCACAC CTACCCTTGC ACACCCACAT TCCTCACCCA 120
TTGCACACAC CTACCCGTGC ATGCCTGCAC CCCTCACTTC TGTACACACC TACCCATGCA 180
TGCCTGCATC TTCGTTATAC ACACCCTACT CATGCACACC CACACCACTC ACCCCTGTGC 240
ACACCTACCC ATACATGCCC ATAGCTCTCA CTGCTGTGCA CAGACCTATC ATGCACACCC 300
ATACTGCTCA CCCCTGTGCA CTCACACCCC CACCCCTGTA CACACATCTA CCTGTGCACA 360
CCCACATCCC TCACCTCTTA CCCCACACAC ACAGCTACCC ATGCACACCC ACACTGCTCA 420
CCCCTGTGCA CACCTACCTG TGCACGCCTG CACCCCTTGA GCCCACAGTT CTTGTGGGGT 480
TGGTGGGCCA CCAGCTGGGC ACCCTCTGTC CCCAGTGGTG AGAGGCAGGT GATGGGGGGG 540
TGAGGCTATG CTCCCTAGTA TCAGGCATTT GGACTGGATT CTGCAGACCG AGCCAGCAGG 600
GCTCAGGGGT TGGTGGTTTC TGATGAAACC TGATTTGCGC CTTTGGCAGT CAGTGCAGCG 660
GGTAGGCAGA AGTCTGGGAG GAGGACAGCT GCACGAGGGT CCGCGTGGGT CCGGTGGGCA 720
CAAAGGGAAG GGAAGGAGCG AGAGTGAGAA AGTGCCTGGT GGGGTGTGGA GGGGTCGGGG 780
TGGGGTATCC AAGCCTGAGG CCCCAGACTT GAGTTCTGGT TAGACAGGGG TGTATCCGGG 840
GATCAGGCTC TCGGCTCCCA CCTCGGTCCA GGAGGGGTCA CCCTGCCACC CCCAGCTTTG 900
GCCCCATGTC TGCTGTGTTC TGCTGTCAGC CCACACATCT GTGTTGTACA GCCGCAGCTG 960
CCGGTGTCTG GTTGGGATGC AGGTCCGCCC AGAATGGAAG ACCGCTGGGG ACTGGGAAGC 1020
TTTCCAGAAA GCCATCTGAG CTCCCCAGAG CACCTGTCAG TGTCCAGACT GTGAAACACA 1080
TGCAGCTGGT GACAGCCAGT GTGGGGCTGT CCCGGAGGTC ATGACAGGTG CAGCCAGCTG 1140
GGCAGCCTGG CTCCTTGGCT CCGTTAGAGC GAGGGCAGCA CATTGTGGGG ACCAAGGAGG 1200
AGTTCAGGGC CGGCAGCAGA TGGGGACTGC CTGGTAGCAG ATGCCCCTGC CTCAGCAGCC 1260
CCTGGGTGTG TCCCTGGGTC AAGAGGGAGT CCCCAGGGAG GGGTAAGGCG TGTGTGACAC 1320
ATCTCAGGGG CCCTGCATCC CCAGCGCAGT GTGCACATGG TTCCCTATGG GTAACTGGCC 1380
CCAGCGCAGT GTGCACATGG TTCCTGACGG GTGACTGGCC CCAGACCCTC TGGCCCCCCA 1440
GCAGTGTAAG CAGCTGGGGG CCATGACGCA GAGGCCCCCT GGGCTTCCGC AAGGATGGAA 1500
AGAGCTTGGG TGGAGGGCCC AGGAAGGAGA CTGTGGGCAT GAGGGCCAGC GCCCTGACCT 1560
GAGGGCACTG GACACTGCTT CTGTTCACTG CTGCCATCAG GAAGGGCTGG GCTGCCGGCT 1620
TCTCAGAGGG AGTCAGGAGT GAGATTCTAT CTGAAATATA CAATTTCCCT CCTGGTCATT 1680
AAGGCAAACA AACTAAAATG CCGCAGGGAC CATGTAGATT GCAGTGGCTG CCCACCCCCA 1740
GGGCCACCCA TTTGTGGCCT GAACCATTTA CCAGCCTTGG AGGTGGCTGG ACCCAGGTGT 1800
GGGCTCCCCC TGGCCTCCTG CCCTCTGTTG GATGCGCTCT GGGGTCGGGA AGGCCGGGGC 1860
AGGGTTGCAG GACGGAGGTG GGGGGCCCCC ACCATGCCCC AGGGGATGAG CCTCTGAGTA 1920
CATCAGAGGG GAGAGAGGAG GGGCCAGGCA GGGAGGAGGG GCCAGGCAGG CAGGGAGCCT 1980
CTAAGCACTT GTGGGAGGAG GTGGGGCCAG GCAGGGAGGG GCCAGTGAGC CACCTCGGAA 2040
CTCAAGGTAG TCAACATTCC CCACAGAGGC GGGGCCCTGG GCTGCCACAG GGCCAAGCTG 2100
GGAGGTGATG CCAGGGCCTG CCCCAGAGTC CAGCCTCTCC TGGGCTGCCA GTTCTCTGCT 2160
TTTCACACTG GGGGCCCCAG CAACACAGGG TCTGACCTCT CGCTCCCTCC 2210
|
