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

TagContent
EnhancerAtlas ID
HS187-06235 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr12:109250000-109251200 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs987044chr12109250356hg19
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00113chr12:109244424-109251439Adipose_Nuclei
SE_01037chr12:109249271-109251865Adrenal_Gland
SE_01623chr12:109246181-109252083Aorta
SE_02246chr12:109246168-109252078Astrocytes
SE_04650chr12:109249244-109251148Brain_Anterior_Caudate
SE_06218chr12:109246114-109251372Brain_Hippocampus_Middle
SE_08617chr12:109249226-109251457Brain_Inferior_Temporal_Lobe
SE_09493chr12:109247147-109253018CD14
SE_25830chr12:109244536-109251201Duodenum_Smooth_Muscle
SE_26704chr12:109246214-109251864Esophagus
SE_29719chr12:109249196-109251365Fetal_Muscle
SE_32104chr12:109249273-109251984Gastric
SE_34450chr12:109246280-109252128HCT-116
SE_34725chr12:109245953-109252240HeLa
SE_36100chr12:109246988-109251401HMEC
SE_36924chr12:109244176-109251762HSMMtube
SE_37947chr12:109244148-109252158HUVEC
SE_38903chr12:109246069-109251429IMR90
SE_40657chr12:109245919-109253030Left_Ventricle
SE_42149chr12:109245912-109252798Lung
SE_44139chr12:109246155-109251395NHDF-Ad
SE_44751chr12:109244532-109252762NHLF
SE_45545chr12:109244280-109252952Osteoblasts
SE_47346chr12:109244433-109251321Panc1
SE_48097chr12:109245995-109252101Psoas_Muscle
SE_48602chr12:109245944-109251883Right_Atrium
SE_49578chr12:109249348-109251413Right_Ventricle
SE_50432chr12:109246119-109251878Sigmoid_Colon
SE_51142chr12:109244391-109251449Skeletal_Muscle
SE_51706chr12:109246219-109251409Skeletal_Muscle_Myoblast
SE_52666chr12:109246054-109251874Small_Intestine
SE_53376chr12:109245391-109252770Spleen
SE_63492chr12:109246142-109251594HSMM
SE_65195chr12:109247561-109251325NHEK
SE_68566chr12:109231845-109256560TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12109250000109250362
Enhancer Sequence
AGAGATGGTG GGCAAGATTG CGCGACCAGA GGGTCATCCC TGCAGCTACA GAGGGCTGAC 60
CTGCTCAGAG GCCCAAGGCC CCAGCCTAGG ACAAGCCAGG CCAACCCTGC AGGCTAAGAG 120
GGCAACAGTG CCCTCAATCA ACCCCAGAGG AAAAAGTGGC CAGGCAAACG GACCTGGGCC 180
ACACACAGAC CCACAAAAAC GCGCACAGTG CCAGGACACG CAACCCAGGA ATGCACCTAT 240
GCAATCACCC AGAATGGGTC ACAGCCACAC AGAAAGATAG ATGCACATAA ACACACAGGC 300
CTGAGTGATG TTACAGAAAG GAAAAGCCAG ACTAAGGCTG CACGCACAGA CGTGAAACAC 360
AGCCACACAG AGCCCACAGC ACGCTCGGTC ACCGTCACAC AGTGACACGG GCACGCCTAC 420
AGACAGAACT CCAGAGGCGG CAGGCGGGGA AACAATCTCA CACGTTTGTA GGGGCACTCC 480
CAGATGCCTG TCTCACGCTG GCACAGTCCC CGGACGGCAG GTCAGCAACA GTCACATCTC 540
ACATCGCACA GCCAGGCATA CAGGCAAAGG GCCTAGAACT ACCCCGGCCA CAGGTCTCAG 600
AACCAGCGGC TCACGCAGTC ACCCAATCAA GGGTCCCAGT TGCACATCCA GTCACCCCTG 660
GACCCTGGTC ACACTGCAGA GTCACTCACA AATGGGAGTC CCGACAGACG CACAGTCCTC 720
CCCAGACAGA GGTCAACCCA AGATGGGGGT CACACCTGAA ATCACAGTCC CCACACAATC 780
ACGAGGTCAC ATCTGCACAC ACAGTCTCTG CACAGTCACC CTTAGGGGTC ACAACGCACA 840
CAGTCTCCGC CTAACAGGGG TCACCCCAAG ATGGGGGTAA CCCCCTGATG TGGGTCACAG 900
CGCACACACA GTATCCTGCA GACACTCCCA GAGGGGTCGC ACTGCATACA CAGTCCCTGC 960
AAAGTCGCCC CCCGATAGGG GTCACACCGC ACACAAAGTC CCCGCACAGC TCCCCAAGAC 1020
AGGGTCACAT CGCACACAGT CCTCGCACGG TCACCCCGGT CCGGCTGCCC GGCTCTGTTC 1080
CTACGGCGGG GCCCCGAGGA GCCCGCGCAG CCGCCCCCCT GCCCCGCACG CGCGGCCCCA 1140
GCTCCGGCGG CCTCGGCGCG GCGTCCGGCG GCCCAGGCCG GGCGCGGCGA GCCCGGGGCT 1200