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

TagContent
EnhancerAtlas ID
HS165-06672 
Organism
Homo sapiens 
Tissue/cell
Ramos 
Coordinate
chr18:46453900-46456330 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs12953717chr1846453929hg19
rs7226855chr1846454048hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr18:46456302-46456323TTTTCATTCCTCCCCTCCCCC-6.6
Number of super-enhancer constituents: 57             
IDCoordinateTissue/cell
SE_00297chr18:46453448-46463365Adipose_Nuclei
SE_01041chr18:46454832-46455916Adrenal_Gland
SE_01041chr18:46456013-46457230Adrenal_Gland
SE_01674chr18:46452291-46454730Aorta
SE_01674chr18:46454795-46457486Aorta
SE_02345chr18:46454738-46457601Astrocytes
SE_03502chr18:46454951-46456443Brain_Angular_Gyrus
SE_04121chr18:46453735-46457695Brain_Anterior_Caudate
SE_05251chr18:46453949-46463370Brain_Cingulate_Gyrus
SE_05955chr18:46446481-46480088Brain_Hippocampus_Middle
SE_07264chr18:46454804-46457381Brain_Hippocampus_Middle_150
SE_08312chr18:46454481-46457759Brain_Inferior_Temporal_Lobe
SE_11810chr18:46453779-46456783CD20
SE_23482chr18:46452353-46454689Colon_Crypt_1
SE_23482chr18:46454826-46457336Colon_Crypt_1
SE_24271chr18:46454170-46454639Colon_Crypt_2
SE_24271chr18:46454869-46455900Colon_Crypt_2
SE_24271chr18:46455981-46456352Colon_Crypt_2
SE_25133chr18:46452324-46454646Colon_Crypt_3
SE_25133chr18:46454948-46456370Colon_Crypt_3
SE_26097chr18:46454679-46457645Duodenum_Smooth_Muscle
SE_26908chr18:46454780-46457321Esophagus
SE_27698chr18:46448262-46462356Fetal_Intestine
SE_28705chr18:46448500-46462248Fetal_Intestine_Large
SE_29974chr18:46454741-46457255Fetal_Muscle
SE_31550chr18:46452309-46454743Gastric
SE_31550chr18:46454749-46457674Gastric
SE_36338chr18:46454783-46457097HMEC
SE_37590chr18:46454272-46457483HSMMtube
SE_38707chr18:46454005-46462116HUVEC
SE_41124chr18:46454782-46457228Left_Ventricle
SE_42227chr18:46452277-46457484Lung
SE_43780chr18:46453091-46463232MM1S
SE_44360chr18:46454809-46457592NHDF-Ad
SE_45015chr18:46454989-46457343NHLF
SE_45645chr18:46452288-46478469Osteoblasts
SE_46741chr18:46455082-46455423Ovary
SE_46741chr18:46455614-46455917Ovary
SE_47308chr18:46448347-46478259Panc1
SE_47678chr18:46454814-46455884Pancreas
SE_47678chr18:46455994-46457265Pancreas
SE_48618chr18:46452288-46457335Right_Atrium
SE_50188chr18:46452299-46454769Sigmoid_Colon
SE_50188chr18:46454783-46471671Sigmoid_Colon
SE_52478chr18:46452303-46462338Small_Intestine
SE_53633chr18:46454831-46457362Spleen
SE_55015chr18:46454612-46457335Stomach_Smooth_Muscle
SE_56403chr18:46454904-46456460u87
SE_56982chr18:46455511-46455896VACO_400
SE_59097chr18:46453600-46480091Ly3
SE_62146chr18:46454581-46479860Toledo
SE_62532chr18:46448756-46483085Tonsil
SE_64174chr18:46454801-46457215HSMM
SE_65410chr18:46451879-46454741Pancreatic_islets
SE_65410chr18:46454837-46457609Pancreatic_islets
SE_67202chr18:46453091-46463232MM1S
SE_68537chr18:46428073-46479503TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr184645510346455621
Enhancer Sequence
ATGCATTTCA CACCAACCTC GCATGCAGCC TCCCGGTAAG TTCAGCTCAT CCCTAAAACA 60
GGGTTCCCCC AAGGCCAGCC TCATAAGGTT GCTGTACCAA TTTGATGCAA AAGTGATTGG 120
GGCCAGCTTG TGGAGAGTGC TGCACACACG TTGGTCTCAT CTCTGAGGCT CCTGGGTTCT 180
CCAGCCGCTC AGAAAATGCC CACCAGTCTT CCTGATTGTC TCCACATCCC CACACCCCAT 240
GGTAGAACAG TTCTGGGCCA ATGCCTACAC TTAATAAGCA TTTACTTTGC ATAGGCTGTG 300
TTCTCTAAGT GGCTCATGAC AACCCTCTGA GGCTGCATAC TATCACCAGC CTATCTTAAA 360
AAAAGGGAGT AGTAGGGGTG AGGCACAAGT CACTGGCCGA AGTGCAGAGC TGCAATTCAA 420
GCCCAGAATA TTGCCTGGTG TGAGCTGTGG ACACAGGCCT CTAAAGCCAC CAAGCCCACT 480
GTTCCTCTCC AAAGTGTCCT TCAGAACACA CTTTGGAAAT GCTGCACCAG CTTTTAGAGC 540
TGCGCATGGG GTGCAACTCC CCTGCAGCAA GAAGTGGGGG GTGATACGGC TTTTTTGCCA 600
GCAAGCTGCT CTGTGACCTT GGCCAAGTGG CTTGCCCTCT CAGGGTCTCA GTTTGACCTG 660
TCCATAAATA ATGTAAAGGG GACAAGGGAA GATGGCCCCA TGGGCCCCCT TCTGCCTTCA 720
TGGTCTCTGG CTGGACTCTG ATTCTCAGTA TTAAACAACA CTGGTTCCAT TTATTTTTAC 780
TACCTTCCAG AGAGTAAGAA AACCACTTTG AGGAGCAGGG TACATTTTTG CATTTAATTT 840
GCAACAATAA AACAAAATAA AATCAAAAGG GAAAGGAGGT TTGAGTCAGG TTTTGCTGTG 900
TCCATCTCTA AACCAACTTT TTTTTTTCTT TAATTTCAGA GTCAGAAATG ACTTTTTACT 960
CTGTCTTACT ATTCATCACC CTCAAGAGAC GGTGAGCCCC CAAGAGAGGA TCTCTTTTAT 1020
CACTGTCATC CGTCCACTGT CTGCCCAGGC TTGGTTCCCT GAAGTTTCTC CTCCCATCAC 1080
CGCCCTCCTT GCCACCTCTC CCAAGCCTAC ATATTTCGCA GATCCTGCTG GTCTAGAACA 1140
CTAATTAGTG ACTGTGTCCT TACAAATTAT GTTAAATAAT CAATTCCTAG AACTAAAATG 1200
TACTCCCTGG CTCCCCAAAC TGGTCCCACA CCACCTCCCA AAACCCCCCA AGCATCTGAG 1260
TCTGAAGCCC CCAACCTGGG GATGAATGCT CCTAAGAGCA TTTATCTCGC CATGGAGAAT 1320
GTAATTGAGG GTGGCACGGG GCAGGGGAGG AAAGCCACAC AAATCAAAAG CTCTTGTCTG 1380
TCTCGCCAGT CAGGCTGACG CGGCTTCCTG TGCCCCAGCA TTCAGCCATG CAAATTACAG 1440
CGTGTACCCA GCTGCCTGCA GCCACTGCTG TCTGAGGAGG CCCACTCTGC CCAGGCTCCT 1500
CTGAGAGAGG CCTCAGAGGA AGGGTGGGGA CTCCCGACCC AGCCAACTCC ATTCATAATA 1560
TTGACAGTAA AGGGCCTCTC TGGCTGCTGT TTAGTGTGCA TGCAGTCGAA TCATTTCTCG 1620
AGTTCAAATT TCCAGATACT TCCCCTCCAT GGTACACCAA CCAGGTTCCC ACTGTTACCC 1680
CCCAAGTAAC TCAGAGCAGC TCTCTTCAGA AAGGGGGTTC ACATATTAGC AGGCACAGAA 1740
GCCCTCAGCC CTGCATGGCA TTGTCTGCTC AGCTGCCTTC CCTCTGGGCA TGACCCTGGC 1800
ACCCCCAGGA AGACACAAGG GCTGGGACAA GCATGGAACA GAAAGTCTGT CGTGTCCAAG 1860
AGAAACTACC AAGTCAAGTC TCTTACCTCA CCCACCTACC CACCTGCCAC CCTGAGAGTG 1920
TAGGAGATTC CCCAAATTCC CTATCTGGAT TCCCAACTGG GCAGCTGGCA CTGAATGCTG 1980
ATTCATTCTC TCTCTCTCTC TCTCAATCTC TTTCTCTCTT TCTCTCTCTC TCTCTCTCTC 2040
ACTCACACAC ACACACACAC ACACACACGT TAAAGCATCA TGAAAATCTT AATACAAACC 2100
ACTGCATCAT TAAGCCAATT TTCCAAAAGG ACAAAACCCC TAGAAGGACA GGACAGTTTT 2160
TCCCTGGTTT TGCAGGTGGT GGGGGGGCTC TGTGTGTGCA AGAAACCAAG CTACTTTTGC 2220
TGTGGGCCTC GTTTTAATAA AGCCCCAGGC TACCAGGACC CCTAGTCCTT GGAAGGCATC 2280
ACAGGACCCA AAGGCAGACC CTTCTCCCAC CCTATCCCCC ACAGATCCAA CTCCACTCCA 2340
GTTTCTAGAG GGTAGGAAAA CTGTCCGAAG ACATGGAAAA ATACAGTGAG AAACAAAAGT 2400
CCTTTTCATT CCTCCCCTCC CCCGGCTCCC 2430