EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-70361 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr9:127044050-127046340 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7861040chr9127044135hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:127045265-127045283GGCAGGAAGGAGGGAATC+6.02
KLF4MA0039.3chr9:127046130-127046141CCACACCCTGC+6.62
PLAG1MA0163.1chr9:127044893-127044907GGGGCCACAGGGGG+6.18
SP8MA0747.1chr9:127044914-127044926GACACGCCCACT+6.37
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01861chr9:127043953-127046452Aorta
SE_02294chr9:127043937-127045792Astrocytes
SE_03002chr9:127044065-127045325Bladder
SE_03002chr9:127045330-127046413Bladder
SE_04593chr9:127044035-127046338Brain_Anterior_Caudate
SE_06625chr9:127043834-127049648Brain_Hippocampus_Middle
SE_09789chr9:127043706-127046156CD14
SE_23712chr9:127043999-127046004Colon_Crypt_1
SE_24006chr9:127044045-127046083Colon_Crypt_2
SE_26169chr9:127043599-127046347Duodenum_Smooth_Muscle
SE_27460chr9:127044035-127046123Esophagus
SE_29975chr9:127043997-127046387Fetal_Muscle
SE_31765chr9:127044041-127046389Gastric
SE_36996chr9:127041377-127050527HSMMtube
SE_38009chr9:127039597-127046184HUVEC
SE_38868chr9:127043970-127046447IMR90
SE_42506chr9:127043941-127049998Lung
SE_44293chr9:127044212-127046445NHDF-Ad
SE_44809chr9:127043918-127049996NHLF
SE_45648chr9:127040018-127051411Osteoblasts
SE_47283chr9:127041647-127050279Panc1
SE_47557chr9:127044376-127046209Pancreas
SE_49326chr9:127043970-127046367Right_Atrium
SE_50283chr9:127041756-127046427Sigmoid_Colon
SE_52726chr9:127043913-127046460Small_Intestine
SE_54297chr9:127043843-127046283Spleen
SE_60448chr9:127019058-127056389DHL6
SE_65907chr9:127043647-127046632Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9127044810127045891
chr9127045133127045416
chr9127045925127046114
chr9127044082127044798
Enhancer Sequence
TACAGGCGTA AGCCACCACA CCCGGCCTGT CCTTTCTTTT ATGAAAGATG GTGATACTAG 60
GTGGACGTTT TATTTTAGAT GCCAGAAAAC TCTGGCAACC TATGTCTATC TTCAAAATGT 120
GGGAGAGGCT GTCCAGGCCT GTGACACCTC CAGGCCCGGA AGCCATTGAT GTACTTCTGT 180
ACCCCAGACA CAGAAGTGGA GCCCGGGGCA GACTTTGATG CCTCAAGAAC CTCTGAGTCA 240
TGGCCACACG TGAGCCCCCG GCTCTGCCCT GGTGTGCGGT GGGGCGTATT GGTTTCCTAG 300
GGATATTATA ACAAATTACT GCAAACTGGG TGCTTGAAAA CAATAGAAAT TCATTCTCTC 360
TTGGAGAATC CTGGAGGCGT GATGCCTGAA ATCAGGCTGG TGGTAGGCTC AGTTCCCGTG 420
GAGGCTCTGA CAAAGCACCT GCCGTGCCTT TTTCTGGCTT CTGGCAGGCG CTAGCCACCC 480
TCCTTGTTCC TTGTTCCGTG TTCCGTGGCT CGTCTACACA TCCCTCCAGT GCTCGCCTCT 540
GTCGCCACAT GGCCTTCTTC CTTGTGCGTC TGTCTCTGTG TCCATCCCTC ATAGAAAGAC 600
ACCCGTCATT GAATTTGGGC CACCCTAATC CCATGTGACC CCAGCTTAAC TTGATTAGTA 660
TCTCCAAGTA AGGGCCTATG CCCCAGTTCC AGATAGACAA GGGTTTGGGG GGAACATTAC 720
TCTGGGGGCG TAAGGGATGA GGAGGGCAGG TCCAGGGAGC CTGCCCTCAT TCCCAGGAGG 780
AGACAGGAGA CCAAGGAGCA GAGTCTGGCG GGGGAACGCT GTCACCACAG CAAGGGCCAG 840
GCTGGGGCCA CAGGGGGTGG GTCAGACACG CCCACTGAAT ACTCAGGGGC ACGGGAGGGC 900
CGGGATCCCC CTGACTCTCT GCATCCCAGA TTCATTCCTA CGCTTTCATA CAGGCCCCAA 960
AGACAAGTGC TGAGTAGATC TGGGTCTTCA GCACGATGTT TTTTAAAAAC AGGCTTGCAG 1020
CGTTTGGTCC TTTGGTGGCA CCAGCCAGGA CCACTGAGGG CTGAGAACGT CTCAGCGCCC 1080
AGCATAGGCC GCCAGCCCTG GCTCTGCTCT TTTGGGTTAG AGAGCGGCCC CTCCCAGTAA 1140
TGACAGGGCC CGCCATTCCC GGCAGCGCCC ACCAGCACAG CCTCCCCCGC TTTGTGGACA 1200
AAGGGCAGCC TGTGGGGCAG GAAGGAGGGA ATCCAGCCTC CCCTGTTCCC CCAGAGGCCT 1260
TTATCTATTT TGGCAAAGGC CCTGTGATCA GACGTTTCCG CCCTGACAAC TCCCTGCCAA 1320
GTGATCTCAA GCAAGGGAGT CCCAGAGCCC TGCTGAGCCC CACTTCTCTC CTGTGAAGTA 1380
GGAGGCACAG TTCCAGCCCT GACCCTCTCA GGAAGGCTGG GGATGACAAG GCAAACCCTT 1440
CCCGTGCCTA GCCCAGGGCC TGGCACATAG TAGGTGCTCA GTCAATACTG AATGAGAGAG 1500
AGCATCTTGG AGCCCAGAAC GTAAATTTCA TGCCACTCCT GCGACGGAGC CTCAGTGGGG 1560
CCTCTTGGGA AGGAGAATCT ATAGGCATTT CCTTCCCCAC GTCCTAGGAC ACAGTTAGCT 1620
GAGACGACCG GGCAGGGGTG GGGAAGTTGA GTGCACGGGT GTAGCACTGG ACGGAGGACA 1680
GAGGCTGCTA AGCTGCATCT CAGGCATTGA TTGGCATTGA GGAAAACCCA CCTAGACTTG 1740
GTATCGCGGG AGGGAGGGTC ATGTGCAGGG AGCCCTGGAA GGGAGCCTGG AGAGCTGGGT 1800
GCCAGCCCTG GCTCTGCACC CCTTACCAGC CATGTGCAGG TCATGGCAGT GCCCTGTGGA 1860
TCCTACTTCC TGAACCTCCC CTCTGCAGGC TTGATGCCAC TGCTGTCATT TCGGCCTCTA 1920
TCCCACAACT CGCACAGGGC TTGCCTCACC TTTAGGCCTT TGCACGTGCC ATGCCCTCTG 1980
CCTGGAGTGC CCTGCCCCTA TTCCTCCACT CAGAGCTGCT TCCCGTTCCG AGGAAAAATC 2040
CCATGCCCCA GGTAGACTGC ACGCACATTT TCTTGTGTTT CCACACCCTG CTTTGCAGAG 2100
CAGCGGGCAC CCTGGTTGTA GTTTAAGGGA CGCCTGAGAG CCCCATTGAG GATGGAGATT 2160
GGTCCCCCTT GCCTGGCACA CGCTTGGTGC CCAGCACTTG TGTGTCCATT GAGTGAGCAA 2220
ATAATGGAAT GTCTGGAGGC ATGTGACGCC TCTGCTGTGT GGCTTGGTTT CCCCATCTTT 2280
AAAATACCAG 2290