EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-20328 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr3:50642290-50643780 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs201193chr350643305hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr3:50642694-50642711TGGGTCATGGTGACCTG-6.93
ESR1MA0112.3chr3:50642694-50642711TGGGTCATGGTGACCTG+7.18
ESR2MA0258.2chr3:50642695-50642710GGGTCATGGTGACCT-7.88
Foxo1MA0480.1chr3:50643591-50643602TCTTGTTTACA+6.02
PPARGMA0066.1chr3:50642693-50642713CTGGGTCATGGTGACCTGGA+6.32
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00760chr3:50636720-50645111Adipose_Nuclei
SE_09279chr3:50636789-50643770CD14
SE_12298chr3:50641482-50643281CD3
SE_12298chr3:50643290-50643928CD3
SE_12919chr3:50641667-50644863CD34_Primary_RO01480
SE_13361chr3:50636482-50651600CD34_Primary_RO01536
SE_14184chr3:50641870-50645230CD34_Primary_RO01549
SE_14601chr3:50635365-50652110CD4_Memory_Primary_7pool
SE_16238chr3:50642515-50643813CD4_Naive_Primary_7pool
SE_16582chr3:50643134-50650193CD4_Naive_Primary_8pool
SE_17166chr3:50643167-50644034CD4p_CD225int_CD127p_Tmem
SE_18495chr3:50635603-50652144CD4p_CD25-_Il17-_PMAstim_Th
SE_19130chr3:50636430-50651976CD4p_CD25-_Il17p_PMAstim_Th17
SE_20626chr3:50637316-50651753CD56
SE_20911chr3:50636515-50652055CD8_Memory_7pool
SE_25135chr3:50642358-50643042Colon_Crypt_3
SE_25369chr3:50635253-50654453DND41
SE_26772chr3:50636910-50645175Esophagus
SE_28892chr3:50642813-50644572Fetal_Intestine_Large
SE_31573chr3:50636327-50646177Gastric
SE_40028chr3:50636324-50651737K562
SE_40824chr3:50635650-50651738Left_Ventricle
SE_42458chr3:50635760-50651762Lung
SE_47024chr3:50641595-50643846Ovary
SE_47758chr3:50641585-50643943Pancreas
SE_48262chr3:50636469-50651773Psoas_Muscle
SE_49250chr3:50636324-50643972Right_Atrium
SE_49448chr3:50640978-50643949Right_Ventricle
SE_50378chr3:50636461-50651683Sigmoid_Colon
SE_51369chr3:50636562-50644163Skeletal_Muscle
SE_52764chr3:50636819-50646284Small_Intestine
SE_53704chr3:50641936-50643107Spleen
SE_65451chr3:50636456-50645477Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr35064229850643204
chr35064302950643593
chr35064241850642732
Enhancer Sequence
CCACTTGTTG AGTGGCCGTG GTCAGCCCCT TCCCTGCTCT GAGCCTCGGT TTCCTCATCT 60
GTGTAGCGTG GGTAATATTT GGACTTCACT CCCAAAGTTG TGGTGAGTGC TACATGAGGT 120
GCAAGCCCTC GCCCCATGCC CAGCACCTGG CAGGCACCTT GAGACATTTC TCTCTGTGTA 180
CAAAGCAGTT TTCTGTGCTT CCTCTAGCCA CAGCAGCTTT CTGTCCAGGC TGCAGCACCA 240
GGTGAGGAAC AGCTTGACAC TGGCCCCTCT GTATCCACTA CCCATCCGCT AGGTGACTCA 300
AATCTAGGGG TGAAGCAGAC AGAGGGGTTA CCTCAGGCAT TCTGGAAGCA ATGAAGCAGC 360
TGAAATTCAG ACTGAAGGAA TGAGGAACTG TAAATACCCC TGGCTGGGTC ATGGTGACCT 420
GGAGGAAGCG TGCCATCTGG CCCTACAGAC AGCCAAGCGC TCAGGCCGCC GCCAGTAACA 480
GGGAAGGCAC GTGGCTGGCC ACCTGGGTCT GGGCACCACA TCCAGGAAAG ACAGCCCTCC 540
CTCCATCACC CACCTCTTGC TCACTCTCAC CTAACGTCAG ACCTATTCTT TGCCATGACT 600
GCCTCCATGT CCCCAGGGTC CTGTGTGAAC TCCATGGTTC TTGCTGTCTA TCCTCGTCCT 660
TACCCCTCCC TGTAATCAGC CTGTCACTCC TCACCCCTCC TTGCTCTCAA CCTGCCAACA 720
AGTGTCTCTT CTACTCTAAG ACTTCTAATT GCTTGAGGGC TAAGACAACA GGAAGGTTAG 780
GATTGTTTCC AGAATAAAGG TTAGAAAGCT TTAGAGAAGC TTTCCTGTGG GGCCCTCAAG 840
CAAAGGTGCG GAAAACTTCG GGACACAGGA AGATCTCAAC AGATAGTGTT CCAAAGTCAG 900
ACTGTCCGGT AATGGAGGGT GTTTTCATTG AAATTGCTCT TCCACACACT TTTGGTGTGC 960
TGAACCCTGA GAGAGAAGAA AGGATCCCCC AATCCCAACC AGTCTGGACT AGAACCCGGA 1020
CACCTCCGCC CCAGGTCAGA CTCTGCCAGC TCACTGGCCC CTACCCCGAT TCAATTGCCC 1080
TGCCCCACTG CACAGAGCAA GCCCTCTTCA GTTCTGTGTG TCAGGAACAC GTGCCTCCCA 1140
GTCATGCCTT GGTGCCTTTG CACTCACTGT ACCTTCTTCC TGGGAGAACC AGCCCTGACT 1200
TCTCTGACTA CTAGTTTCCT CATCTCAAGA CACTGACCCC AGGAGTAGTC CACAGCTCTC 1260
TCTCCCTGGG TATTCTCCAC TTGCGATTTG GAGTTGGCAT TTCTTGTTTA CACATCTCTC 1320
AGGGCTGATG CACCTCTGCC ACCCTCCCCC GAGCCCTCGC CTGGCAGTGG CCAGGGCAGT 1380
CACCCTGCAG GCAGTCTAAC TGGCCTTTGT CTCCTAGCTC CCATTTCCCA AGGGGACCCA 1440
GGGGAGATGA GAGGAGAGGC TGCTCCCTGT CTCCTCCACT CCTTAATGAG 1490