EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

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EnhancerAtlas ID
HS184-12703 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr16:81511990-81513000 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56320921chr1681512760hg19
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_00444chr16:81511701-81513693Adipose_Nuclei
SE_01065chr16:81511594-81513103Adrenal_Gland
SE_09239chr16:81509839-81518273CD14
SE_11291chr16:81509731-81518789CD20
SE_23105chr16:81511001-81512714Colon_Crypt_1
SE_23862chr16:81511657-81512683Colon_Crypt_2
SE_26527chr16:81512222-81512842Esophagus
SE_28752chr16:81512728-81513740Fetal_Intestine_Large
SE_31484chr16:81510967-81513134Gastric
SE_38248chr16:81511744-81513512HUVEC
SE_42333chr16:81510302-81513207Lung
SE_50187chr16:81510363-81513965Sigmoid_Colon
SE_52343chr16:81511555-81513890Small_Intestine
SE_53457chr16:81510303-81513992Spleen
SE_65249chr16:81511919-81513158Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr168151260881512902
Number: 1             
IDChromosomeStartEnd
GH16I081476chr168151045681517804
Enhancer Sequence
ATTTTGGCGT CCTGTATGGA GAGGAGCAGC CTGCCGGAGA AGATAGTGAG CTCCCTGAGA 60
AAGCAGGTGT GCAAGCAAAG GTCAGATGGA CATGTGTCAG TCAGGGAGGC CACCGAGTGC 120
GTTCTAGATC CAGAAAGCAC ATTCATGGAA TTCCATTGAG GAATTATGGA AGGGATCTCA 180
TGCAGGGATG GTGAATGCAC AGACCATGTG TGGTCCCCTC CACCCTCCAG CCCTTGTTGG 240
TCCTCCTGGT GCCCTGCAGA GCCGCAGCCA CCCCAGAGCC TCCCGGTGGG AAGAAGTTGG 300
CACCTGAGAT AAACCCATTT GCTTTTCCCA CTTGAATTCA GTTCTCTTGT TCCTATAGGT 360
GTGGACGTTG AGGGCCAGCC TGGAAGCGCC ATATCCAGAG GCACTCAGGG AGGGGAGCAG 420
GAGACCCAGG GCTCTGGGAT TCAGGTCCCT CTGTCACACC CTGCCCTTCT TCTGGGTCTT 480
TCTTCCCCAC CTCCCAGCCA GAAATTGCCT CCTGGAGCCA GCCCAGCCTC GTCTTGTTCA 540
TTGGAGCTCA GTTGGAGACC CGTCCTCACC CGAAGCAGGG TGAGAGGACA GCACCTGCCA 600
CCTTTAAGTC TGGGCTTTGC TGGACGCCTA GGAGAAGCCG GGTCCTCAGG CACTCGAGTG 660
GGAAGTGAAA GTGTGCACCA GCTCTTTAGT TCTGCTATTG ACCGGACAGG GTTTTTCCTG 720
GGGGGAGGGG GAAGGAGCTG CTGTGTTTTC TTTGCTTAAT CTGGCCTTGC CCCACAGAGA 780
AAACACATGC GTAGCCTCCA TCCTGTTTGT AAAGAGGGCG GTCAGCTACT CGAAGTTGCT 840
CGCCTGGAAA AACTGGGAAG ATGTCATCTC CTATGGTAAG GAGGTGGGGG CTACAGGTAG 900
CTGAGGTGGG CAATGAATGT CTTGAGGGAC TGTCAGCATG TGACCTTTTT TTAAATGGTG 960
ATAAAATACA CGTAACATAA AATGGGCCAT TTTAACCAGT TTTAAGTGTG 1010