EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS134-36754 
Organism
Homo sapiens 
Tissue/cell
Mesendoderm 
Coordinate
chr22:36756670-36758680 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs136211chr2236758547hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr22:36756760-36756781AAAAAAAAAAAGAAAGAAAAA-6.59
IRF1MA0050.2chr22:36756766-36756787AAAAAGAAAGAAAAAGAAAAA-6.68
Nr2f6(var.2)MA0728.1chr22:36757898-36757913GAGGTCAGGAGTTCA+6.22
PRDM1MA0508.2chr22:36757483-36757493TCACTTTCAC+6.02
ZNF263MA0528.1chr22:36757210-36757231CCCCCTTCCCTTTCCACCTCA-6.09
Number of super-enhancer constituents: 60             
IDCoordinateTissue/cell
SE_00116chr22:36744550-36773501Adipose_Nuclei
SE_00874chr22:36756697-36757690Adrenal_Gland
SE_01541chr22:36756672-36757952Aorta
SE_01541chr22:36758001-36762083Aorta
SE_02243chr22:36756652-36757859Astrocytes
SE_02896chr22:36756802-36757908Bladder
SE_05865chr22:36756326-36761563Brain_Hippocampus_Middle
SE_09195chr22:36744556-36774047CD14
SE_10697chr22:36756800-36757861CD19_Primary
SE_11020chr22:36744527-36785336CD20
SE_11868chr22:36756699-36757969CD3
SE_11868chr22:36758007-36758669CD3
SE_13866chr22:36756805-36758676CD34_Primary_RO01536
SE_14476chr22:36756786-36757863CD4_Memory_Primary_7pool
SE_16932chr22:36756964-36757891CD4p_CD225int_CD127p_Tmem
SE_16932chr22:36757992-36758699CD4p_CD225int_CD127p_Tmem
SE_17339chr22:36756664-36780212CD4p_CD25-_CD45RAp_Naive
SE_17788chr22:36746596-36785463CD4p_CD25-_CD45ROp_Memory
SE_18286chr22:36744506-36778586CD4p_CD25-_Il17-_PMAstim_Th
SE_19119chr22:36756666-36778387CD4p_CD25-_Il17p_PMAstim_Th17
SE_20220chr22:36756688-36757984CD56
SE_20220chr22:36758098-36763991CD56
SE_21957chr22:36756540-36757850CD8_Naive_8pool
SE_22328chr22:36756666-36770326CD8_primiary
SE_23071chr22:36756789-36757919Colon_Crypt_1
SE_23071chr22:36758133-36758683Colon_Crypt_1
SE_23740chr22:36756795-36757549Colon_Crypt_2
SE_25782chr22:36756588-36771936Duodenum_Smooth_Muscle
SE_26521chr22:36756697-36758025Esophagus
SE_26521chr22:36758036-36775377Esophagus
SE_27650chr22:36756641-36761849Fetal_Intestine
SE_28644chr22:36756100-36761903Fetal_Intestine_Large
SE_30956chr22:36756775-36757644Fetal_Thymus
SE_31378chr22:36756746-36757946Gastric
SE_31378chr22:36758108-36762068Gastric
SE_35832chr22:36756767-36768386HMEC
SE_37948chr22:36745836-36771974HUVEC
SE_40597chr22:36756652-36770124Left_Ventricle
SE_41574chr22:36756793-36757576LNCaP
SE_41574chr22:36758071-36758664LNCaP
SE_42094chr22:36756687-36757946Lung
SE_42094chr22:36757994-36770152Lung
SE_44762chr22:36756662-36757927NHLF
SE_44762chr22:36757965-36758680NHLF
SE_45604chr22:36756644-36768407Osteoblasts
SE_47169chr22:36744668-36771991Panc1
SE_47463chr22:36756741-36757565Pancreas
SE_48566chr22:36756719-36761708Right_Atrium
SE_50050chr22:36756680-36761699Sigmoid_Colon
SE_51217chr22:36756632-36757724Skeletal_Muscle
SE_51217chr22:36758477-36761577Skeletal_Muscle
SE_52340chr22:36756669-36762077Small_Intestine
SE_53283chr22:36756728-36758683Spleen
SE_54489chr22:36744394-36771971Stomach_Smooth_Muscle
SE_55761chr22:36758025-36763029u87
SE_58448chr22:36724049-36832686Ly1
SE_62244chr22:36719186-36785326Tonsil
SE_65307chr22:36756313-36764221Pancreatic_islets
SE_67526chr22:36758025-36763029u87
SE_68689chr22:36755117-36757853H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223675821236758558
Enhancer Sequence
TGGCGTGAAC CTGGGAGGGG GAGCTTGCAG TGAGCCGAGA TCGCACCACT GCACTCTAGC 60
CTGGGCAACA GTGTGAGACT CCATCTCAAA AAAAAAAAAA AGAAAGAAAA AGAAAAAAGA 120
AATCTGCTTA ACTCCATCCC AGGAATATCC TGCAGGAAAA ACCTCTCTCC ATGCTGGTCT 180
GGGAAATGCT GGTCTGGTGA GATGGGCACA AAGCCTGTGG CAGAAGAGCT GGATTTGAGT 240
CCAGCGAGGT GCTGACCAGC TGTGCAATCC TGCAGGCACC ACCCAGGCCT CGGCTTTCCC 300
ACCTGCAAAA TGTCCTATCT GCTCACAGGT ATGCACAAGG CCACTCTCTG CAATACACAC 360
CAGGGCTGTC AGAGCAGTTA TCTACAGGGT GGGTCAATAA AGTGGCTCCT CTGTCACCCA 420
GGGCTAATAA CCTACAGCAG CCTCGACCTA GGCCCTCACT CTCCCCAGGC TAACAAGGAG 480
TGGGGGGCTC CTCCCAGCTG CCAGTGCCCA GGAGGTAGGA GCTGAAGACT GCGGGTGGGC 540
CCCCCTTCCC TTTCCACCTC AGGAATGTTG TTTGCTTACA GAAGAAGCTG GAACTTGTTT 600
CCATTAGCAG TATTCCAACC CAAGCCTGTG TTGATGCTTA GCAGATAAGA AAACCAGAGA 660
GGAACTTAGT GCCCGGGCCC CAGAGCCTGC CCCATCTGCA GGTTCTGCCT TTGCCTCCTT 720
GAAGCGGGCA TGGAGGGGGG CTCAGGTGAC TGCTGAAAGT CCAGGAAACA ATGAAAGATG 780
ATGGCATTTG CCTGTCCAAG GGAGGGCCTG TGGTCACTTT CACTTTGCCT GGCACCGAAG 840
GAAACTCAGG CTATCAAAAA CAACACCAGT ACGTATTTCA AATCATGTTG TACACAATGG 900
ATATAAACAA TTTTTGTCAA CTTAAAAATT AAATGAACAA TTTCTTTTAA AAAAAAAATG 960
ACACCAGAAA CCAGAATGTG GTACATAGAG TCCCTCCTCC TGCATGGGAA GGGGTGGGGG 1020
CAATAGCTTG GGACAGGCTG GAGGAGATAA ACTGGGGCAG CTAACCCAGG ATCTTATCAG 1080
CCATTTAGGA ATGTGGACTT TATTCTAGGG ATAATTGGGG AGGAGCAGAG GTGACATCAG 1140
ATTTGTATTT TAAAGTAATT GGCTGGGGGT GTACGGTGGC TCACGCCTGT AATCCCAACA 1200
CTTTGGGAGG ACAAGGCAGG TAGATCACGA GGTCAGGAGT TCAAGACCAG CCTGGCCAAC 1260
ATGGTGAAAC CCCATCTCTA CTAAAAATAC AAAAATTAGC CAGGCGTGAT GGTGTGCGCC 1320
TGTAATCCCA GCTACCCGGG AGGCTGAGGC CAAGAATTGC TTGAACCCAG GAGGCAGAGG 1380
TTGCAGTGAG CCGAAATTGC GCCACTGTAC TCCAGCCTGG GGGACAGAGC GAGACTCTGC 1440
CTCAAAAATA AAAAAAACAG AAATCATCCT CCCTTACCTG CATGGAGGGG GCAATGAGAA 1500
GTCAGTGGTT GGAAAATACT GGGGACTTGC AAGGAGGGAG CTTCCAATCT AAGAGAAGAA 1560
AAGACAGTTC CCTGACCAGG CTAGGTGGAG AGTGATTAAA TGACACGAGA GGGACAAGTG 1620
CAGCCATAGA CTTTACCCTC TGATCTCCTA CTCCATAGAG CCTGGCTCGA GGAGAGTCCT 1680
GGAATCACCG TCCTACGACA GTGAGAAGTG ACCAAGCAAT CCCAGGAGCT CCAGGGCCAG 1740
TGTTTCCAGA GCATCTTAGG CACAGATCTC ATGTGGCATG TGTCACACAG ACTACACAAT 1800
AAAGTGTCCA ATGGGGTGTC CTCCACTAAG ATACCAACTT CAGGACCACA GAGACATGGC 1860
TTTAGATCCT CAGCACAGAA ACCATTTCTG AGTCGCTCTG TTGCCCGGGC TGGAGTGCAG 1920
TGGCACAATC TTGGCTCACT GCAACCTCTG CCTCCTGGAT TCAAGTGATT ATCCCGCCTC 1980
AGCTGGGACT ACAGGTGCAT GCCAGCACGC 2010