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

TagContent
EnhancerAtlas ID
HS099-15473 
Organism
Homo sapiens 
Tissue/cell
HSMMtube 
Coordinate
chr3:50285610-50287210 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2298952chr350286953hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EsrrgMA0643.1chr3:50286133-50286143ATGACCTTGA-6.02
IRF1MA0050.2chr3:50286228-50286249GAGGGGAAAATGAAACTTGAA-6.21
RORAMA0071.1chr3:50286134-50286144TGACCTTGAT-6.02
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00328chr3:50272275-50294504Adipose_Nuclei
SE_00924chr3:50285666-50287046Adrenal_Gland
SE_01672chr3:50284685-50287092Aorta
SE_02846chr3:50285577-50286779Astrocytes
SE_03917chr3:50285788-50288246Brain_Anterior_Caudate
SE_04864chr3:50278146-50288370Brain_Cingulate_Gyrus
SE_05809chr3:50271925-50313735Brain_Hippocampus_Middle
SE_06748chr3:50285481-50287184Brain_Hippocampus_Middle_150
SE_07819chr3:50273449-50289446Brain_Inferior_Temporal_Lobe
SE_09475chr3:50273514-50296642CD14
SE_13800chr3:50285674-50287008CD34_Primary_RO01536
SE_17710chr3:50272093-50288404CD4p_CD25-_CD45RAp_Naive
SE_18113chr3:50272067-50287604CD4p_CD25-_CD45ROp_Memory
SE_18975chr3:50273503-50289925CD4p_CD25-_Il17-_PMAstim_Th
SE_19368chr3:50281643-50288383CD4p_CD25-_Il17p_PMAstim_Th17
SE_22929chr3:50281635-50287445CD8_primiary
SE_23202chr3:50285581-50286986Colon_Crypt_1
SE_23879chr3:50285586-50286178Colon_Crypt_2
SE_23879chr3:50286180-50286903Colon_Crypt_2
SE_24968chr3:50285688-50286873Colon_Crypt_3
SE_26040chr3:50285735-50287016Duodenum_Smooth_Muscle
SE_26665chr3:50285511-50290083Esophagus
SE_29626chr3:50285527-50287062Fetal_Muscle
SE_31450chr3:50285500-50288273Gastric
SE_34350chr3:50281572-50287028HCT-116
SE_34830chr3:50282763-50288102HeLa
SE_36596chr3:50282561-50287261HMEC
SE_38192chr3:50273512-50288122HUVEC
SE_40718chr3:50282578-50288388Left_Ventricle
SE_42127chr3:50271906-50288361Lung
SE_45312chr3:50285574-50286771NHLF
SE_48477chr3:50282625-50288375Psoas_Muscle
SE_48622chr3:50282644-50288331Right_Atrium
SE_49541chr3:50285655-50286831Right_Ventricle
SE_50198chr3:50282598-50288279Sigmoid_Colon
SE_52519chr3:50282642-50288279Small_Intestine
SE_53321chr3:50271955-50288381Spleen
SE_57397chr3:50286092-50286932VACO_503
SE_62832chr3:50263305-50298785Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr35028577750286185
Enhancer Sequence
GGAGGCAAAG GTTGCAGTGA GCCAAGATCA TGCTATTGCA CTCCAGCCTG AGCAACAGAG 60
CGAGACTGTG TTTCAAAAAA AAAATCTGGA CTCAGCCACC CCTCTGAGAG GCAGGTGCGA 120
GGGGAGCTGG GTGTGTGCAA AACTCACAGA TAAGCCTCTT GCCAGCTTAT CTGGTAGGGG 180
GCATCCCTCA GGTCCTGATG GAAAGAGGAC CCAGCCAGAG ATGGGGAGAG TGAAGCTACT 240
ACCCCACAGC TGCCAGGGCA CTTAGCCTGT GGGCTGCCCG AGAGCTCTTC ACCCCACCCA 300
TTCCACCCAG ATGCCATCCT GGGGCTCCAC CCACCTCTGC TCCTGTCCCC CTTCTCTGCT 360
GGAGCTGCTC CTGGGCTGTG CCCCTGCCTC TGTCCCGTTG TTCCCCCTGC TTCCTGCCTG 420
GCTGCCAGCA CCACACCCTT GTCCTGCCAC TCACTACTTC CCGCCTGAGT CACAGCTGCT 480
GGAAAGACAA AGAGACCAGC CTGAGTCTAG GGATAGGGGC TCCATGACCT TGATTTGCTT 540
ACCTGTCAAG TGGAACTCTT TTTTCAGTGA CCCCTGCTTG GGATAGAGAA TGTTCTCTTA 600
ACATTTAAGA GGCCTTAGGA GGGGAAAATG AAACTTGAAG GGGACAGGGA AGTGGGCCCT 660
CCCTGGCTGG GGCAGGGAGC AGATATCCTG GCTCCTAGTG TGACTGGCTC TGTGCTGCCT 720
ACCTCATGTC TACCAGGTCT AGCTGCTGCT AGGAAAATCA GATGCAAAGC AAGTTTGCAC 780
CCTCGTCCCT GGGCAGGGTC ACGAAGCGGC CCACATCACC TACTAAGAGT GGGCAAAAGG 840
CCAGACCCCC TCTTCACTCT CAGTGGCCAG ATAGGGAAAC TGATGCCTCA AGTGGGCAGG 900
AGTCCCGAAG TCACACAAGA TGGGGAAGCT TTCACCCTAG ACCTCAGGTC CCCCATGCCC 960
TGGGTAGCTT CCCTGCTGAG TCTGAGCTCG CCTGGCTCGG GACTGCATGG GGACCCATGA 1020
CTTCGCATCC TTGGCCTCTG CTCCTGCAGT TCCCCCCATC CTGGCTGTGA CTGGCTCCTG 1080
GTTCTTCCTC CTGCTCTGGA GGAGCCAGTG GGGAAGACAG TCAGGTAGCC ACTGCTGCCC 1140
TCCCTGCCCC AGTGGGTGCT TTGAGCCCCA GGGGGATGGG CCTTAAGTGT TCAGGCATCG 1200
CTGTGAGGCT TTCCTGGGAC CTTTCCCCAT GTCCTCATTG GCAGGTGGAG GAGTGTTGGT 1260
ATGCAGATCC TGGCTGCCCC TTTGCCATGC ACAGCCCAAT GGGGAGGGAG TGGTGCTGGT 1320
ATATATCCCG GTACACACCC CAGTGAAGAT ACTGGGCCCG GCCCCTGTAG TGCCCAGGGG 1380
CTAAAGCAAT AGAGGGGATT GCTGCCCCAG CCACAGCGCC CCAGCCTTCC CAGGGCCTGC 1440
ACATTTGTAT GTCCACAAGA TTGTGCAACC ATCACTGCTA TCTAATTCCA GAACATAATC 1500
ACCACCCTCA AAAATAAACT TCATACCCAA CTAGCTGTCA CTCCCCATCT CCCCAGATCC 1560
CCTCCCCTCA TCCTGGAAAG CAGGCCTGGG ACAGTCAGAA 1600