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

TagContent
EnhancerAtlas ID
HS068-05678 
Organism
Homo sapiens 
Tissue/cell
GM18526 
Coordinate
chr9:127042760-127044510 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7861040chr9127044135hg19
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_01861chr9:127041756-127043926Aorta
SE_01861chr9:127043953-127046452Aorta
SE_02294chr9:127041734-127043104Astrocytes
SE_02294chr9:127043937-127045792Astrocytes
SE_03002chr9:127041823-127043169Bladder
SE_03002chr9:127044065-127045325Bladder
SE_04593chr9:127044035-127046338Brain_Anterior_Caudate
SE_06625chr9:127041509-127043638Brain_Hippocampus_Middle
SE_06625chr9:127043834-127049648Brain_Hippocampus_Middle
SE_09789chr9:127043706-127046156CD14
SE_23712chr9:127043999-127046004Colon_Crypt_1
SE_24006chr9:127044045-127046083Colon_Crypt_2
SE_26169chr9:127040868-127043262Duodenum_Smooth_Muscle
SE_26169chr9:127043599-127046347Duodenum_Smooth_Muscle
SE_27460chr9:127041771-127043821Esophagus
SE_27460chr9:127044035-127046123Esophagus
SE_29975chr9:127041731-127043291Fetal_Muscle
SE_29975chr9:127043997-127046387Fetal_Muscle
SE_31765chr9:127041848-127043061Gastric
SE_31765chr9:127044041-127046389Gastric
SE_36996chr9:127041377-127050527HSMMtube
SE_38009chr9:127039597-127046184HUVEC
SE_38868chr9:127041773-127043793IMR90
SE_38868chr9:127043970-127046447IMR90
SE_42506chr9:127041753-127043788Lung
SE_42506chr9:127043941-127049998Lung
SE_44293chr9:127041757-127043818NHDF-Ad
SE_44293chr9:127044212-127046445NHDF-Ad
SE_44809chr9:127041738-127043771NHLF
SE_44809chr9:127043918-127049996NHLF
SE_45648chr9:127040018-127051411Osteoblasts
SE_47283chr9:127041647-127050279Panc1
SE_49326chr9:127041787-127043648Right_Atrium
SE_49326chr9:127043970-127046367Right_Atrium
SE_50283chr9:127041756-127046427Sigmoid_Colon
SE_52726chr9:127041767-127043867Small_Intestine
SE_52726chr9:127043913-127046460Small_Intestine
SE_54297chr9:127041784-127043103Spleen
SE_54297chr9:127043303-127043836Spleen
SE_54297chr9:127043843-127046283Spleen
SE_60448chr9:127019058-127056389DHL6
SE_65907chr9:127041740-127043255Pancreatic_islets
SE_65907chr9:127043647-127046632Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9127043634127043741
Enhancer Sequence
CCTGGAGTTG CTGGAGAAGA AACATTCCTC ACGCTCATGC GAATGTTTCC CTGGGCTGCT 60
GTCCCAGCAC TGGGTACCGT GGGGCAGACA TGGGTGTGAC GTTTTCCAAG CACGAGGTGA 120
CCAGTGTCCA TTGGGTCATC AGGCCTCCAG GGCCACATGT TTGGAAAGCT ATTCCTGGAG 180
CACCAGGCAT CTGGCACCTC GCTCTGTGGC TAGGCACGGG TTTATGAGGG GACCCTGCAG 240
AGAGCTGGGG TCCTCAGCCT TGACATTTGC ACATTGTGTA TAATTTCACG CTTTGCTTTG 300
CTTTTTTCTC TTCATTTTTT TCTTTTTTTG AGACAGGGTC TTGCTCTGTT GCCCAGGCTG 360
GAGGGTAGTG TCGTGATCTC GGCTCACTGC AGCCTTGACT TCCTGGGCTC AAGGGATCCT 420
CCCACCTCAG CCTCCCAAGC AGCTGGTGCT ACAGGTGCAT GCCACCACAG CTAATTTTTG 480
TATTTTTTGT GGAGATGGGG TTTCTCCACA TGTTGGCCAG GCTGGTCTCG AACTCCTGAC 540
CTCAGGTGAT CCACCCACCT CAGCCTCACA AAGCGCTTTT GTTTTTCTTG AGAAAGATCA 600
GAGCTTCCCT GCTGCATCTC CCGCTTTTCG CTTGTGTTTT CTTTTCTTCC TCACCAGCAG 660
GCTGCCTGGT GACTGGCCTG GGGGCCTCTT CCCTCAGACC AGGAAATCAC CCAGTACTCC 720
GAGAGTGTTC ACTAGAATTA CCCTCATGTT CACTGGAATA TACTGGTCAG ATTTCTGAGA 780
GGGAGACCCC CTTTTTGTAC TCATAGGAGA ATGGAGGAGG CCGGCCATGC TTCTCCTCAG 840
CCACGATTGA AAAAGTCACC TAGCACAGTG GCCTGAGTCC ACTGGTTCCC AAATCCCAGA 900
CCCAGGCCAG GCCTAGGGCC GTGTGAAGTC TTCCGCGGAC CCACGGTGAA ATAAGAAAAG 960
GAAGGCCTGG CTTGGCATAG CTACTTTCCA TGTCAGCTGT TTTTTCTTTT TTTTTTTTTT 1020
TTTTTTTTTT TTTTTTGGAG GCAGAATCTC ACTCTGTCGC CCAGACTGGA GTGCAGTGGT 1080
GCGATCCCAG CTCACTGCAA GCTCCACCTC CAGGGTTGAA GTGATTCTCC TGCTTCAGCC 1140
TCCTGAGTAG CTGGGATTAC AGGTGCCTGC CACCACACCC AGCTAATTTT GTATTTTAGT 1200
AGAGACAGGG TTTTACCATG CTAGCCAGGC TGATCTCGAA CTCCCGACCT CAGGTGATCT 1260
GCCTACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTA AGCCACCACA CCCGGCCTGT 1320
CCTTTCTTTT ATGAAAGATG GTGATACTAG GTGGACGTTT TATTTTAGAT GCCAGAAAAC 1380
TCTGGCAACC TATGTCTATC TTCAAAATGT GGGAGAGGCT GTCCAGGCCT GTGACACCTC 1440
CAGGCCCGGA AGCCATTGAT GTACTTCTGT ACCCCAGACA CAGAAGTGGA GCCCGGGGCA 1500
GACTTTGATG CCTCAAGAAC CTCTGAGTCA TGGCCACACG TGAGCCCCCG GCTCTGCCCT 1560
GGTGTGCGGT GGGGCGTATT GGTTTCCTAG GGATATTATA ACAAATTACT GCAAACTGGG 1620
TGCTTGAAAA CAATAGAAAT TCATTCTCTC TTGGAGAATC CTGGAGGCGT GATGCCTGAA 1680
ATCAGGCTGG TGGTAGGCTC AGTTCCCGTG GAGGCTCTGA CAAAGCACCT GCCGTGCCTT 1740
TTTCTGGCTT 1750