EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS043-19743 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chr18:46448790-46452080 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs7229639chr1846450976hg19
rs12956924chr1846451146hg19
rs4939567chr1846451873hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr18:46450258-46450269GGTGACTCATC+6.32
JUN(var.2)MA0489.1chr18:46450254-46450268AGAAGGTGACTCAT+6.98
JUNDMA0491.1chr18:46450258-46450269GGTGACTCATC+6.62
KLF5MA0599.1chr18:46449216-46449226GCCCCGCCCC+6.02
MNX1MA0707.1chr18:46451962-46451972TTTAATTACC-6.02
STAT1MA0137.3chr18:46451326-46451337TTTCTGGGAAA+6.02
STAT3MA0144.2chr18:46451326-46451337TTTCTGGGAAA+6.32
ZIC4MA0751.1chr18:46449697-46449712ACCCTGCAGGGGGTC-6.02
ZNF263MA0528.1chr18:46450576-46450597GAAGGAGGCGGGAGGGAGGGT+6.05
ZNF263MA0528.1chr18:46450579-46450600GGAGGCGGGAGGGAGGGTGGG+6.26
ZNF263MA0528.1chr18:46450674-46450695ACAGGAGGAGGAGGAGGAGGA+6.27
ZNF263MA0528.1chr18:46450686-46450707GGAGGAGGAGCAAGGGAGTGA+6.29
ZNF263MA0528.1chr18:46450680-46450701GGAGGAGGAGGAGGAGCAAGG+6.65
ZNF263MA0528.1chr18:46449137-46449158GCCCCCTCTCTCCCCTCCTTC-7.29
ZNF263MA0528.1chr18:46450683-46450704GGAGGAGGAGGAGCAAGGGAG+8.21
ZNF263MA0528.1chr18:46450677-46450698GGAGGAGGAGGAGGAGGAGCA+9.2
ZfxMA0146.2chr18:46449213-46449227CAGGCCCCGCCCCG-6.18
Number of super-enhancer constituents: 55             
IDCoordinateTissue/cell
SE_00297chr18:46448577-46450583Adipose_Nuclei
SE_00297chr18:46450614-46453330Adipose_Nuclei
SE_01041chr18:46448918-46450329Adrenal_Gland
SE_01041chr18:46450406-46451733Adrenal_Gland
SE_01674chr18:46446576-46452232Aorta
SE_02345chr18:46448609-46451747Astrocytes
SE_02959chr18:46449452-46450546Bladder
SE_03502chr18:46450845-46451754Brain_Angular_Gyrus
SE_04121chr18:46446479-46452228Brain_Anterior_Caudate
SE_05251chr18:46445014-46452013Brain_Cingulate_Gyrus
SE_05955chr18:46446481-46480088Brain_Hippocampus_Middle
SE_07264chr18:46445463-46450598Brain_Hippocampus_Middle_150
SE_07264chr18:46450956-46451885Brain_Hippocampus_Middle_150
SE_08312chr18:46445207-46450211Brain_Inferior_Temporal_Lobe
SE_23482chr18:46448932-46451606Colon_Crypt_1
SE_24271chr18:46449078-46450285Colon_Crypt_2
SE_24271chr18:46450887-46451277Colon_Crypt_2
SE_25133chr18:46448916-46450473Colon_Crypt_3
SE_25133chr18:46450592-46451617Colon_Crypt_3
SE_26097chr18:46449011-46450489Duodenum_Smooth_Muscle
SE_26097chr18:46450517-46452132Duodenum_Smooth_Muscle
SE_26908chr18:46448966-46450150Esophagus
SE_26908chr18:46450605-46451710Esophagus
SE_27698chr18:46448262-46462356Fetal_Intestine
SE_28705chr18:46448500-46462248Fetal_Intestine_Large
SE_29974chr18:46448780-46452056Fetal_Muscle
SE_31550chr18:46448963-46451653Gastric
SE_36338chr18:46449301-46450170HMEC
SE_37590chr18:46448385-46450313HSMMtube
SE_38707chr18:46448562-46452209HUVEC
SE_41124chr18:46448945-46451564Left_Ventricle
SE_42227chr18:46446626-46452180Lung
SE_43780chr18:46448209-46452260MM1S
SE_44360chr18:46448353-46451788NHDF-Ad
SE_45015chr18:46448986-46450546NHLF
SE_45015chr18:46450684-46451714NHLF
SE_45645chr18:46447941-46452243Osteoblasts
SE_46741chr18:46449026-46449910Ovary
SE_47308chr18:46448347-46478259Panc1
SE_48618chr18:46446632-46452213Right_Atrium
SE_50188chr18:46446638-46452169Sigmoid_Colon
SE_51514chr18:46448683-46450328Skeletal_Muscle
SE_51514chr18:46450616-46452298Skeletal_Muscle
SE_52478chr18:46448171-46452220Small_Intestine
SE_53633chr18:46448733-46452215Spleen
SE_55015chr18:46448811-46450287Stomach_Smooth_Muscle
SE_56403chr18:46449163-46450047u87
SE_56982chr18:46448271-46450526VACO_400
SE_56982chr18:46450591-46451478VACO_400
SE_62532chr18:46448756-46483085Tonsil
SE_64174chr18:46449423-46449910HSMM
SE_65410chr18:46446599-46451689Pancreatic_islets
SE_67202chr18:46448209-46452260MM1S
SE_68537chr18:46428073-46479503TC71
SE_69179chr18:46448923-46450285H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr184645062746451701
chr184644909346449527
chr184645120946451517
Enhancer Sequence
AGGTGTCTAG ACTCTGGGAC CACCTATGCG ATGGTCTCTG GGTGCCTGTC ACCCAGCTCT 60
CAAATCAGTG CCGTGGTCAT GAGGAACCTA TCTGGTAAAA ATAAAAATGA GGGTGGCTTG 120
GGACAAAAAC ATCTATATTC CTAATAGGAA AACAGTCTCA GTGTGTCAGC AGCAGCCCTG 180
TACACAAAGG GTGAATTCAT GTCAAAATGC CAAATCACAA CATGCAGACC GGTATTAACC 240
CGGGCTACCT TAACAAAGCT TCCTCCAGCC CAGACAGAAG ATTATGTGTC TCAAATAGAT 300
GCGTCCCCCT TCTCCCCTTC TCTGCCGGCA CCCCCATCCC CAGGGGTGCC CCCTCTCTCC 360
CCTCCTTCCA CAGAAGCATC TGGAGCCTGC AGGGCGCCCT GCTCCGCCCT CATCCCTCCC 420
CTGCAGGCCC CGCCCCGCTT CCCTACACAG TCTTCCCACA GGCAGCCTGG GGGCCGGGGT 480
GATTCTGGTA AGGTAATTTT CCTCAACAGG CACTTGGAGG ACTTTAAAAG GGGGGTCACA 540
CGGAGGGAAA GGGAGCCCCG GCGGCGGGCA TTCTGACTCC TCCTTAAGTA GGAGCCAGCG 600
GGCAGGCCTC AGACTTGGGA CCATAAATCT CCCCAGCCCA GCCAGACTGC AGGAACGCTG 660
TGGTTTGTGG CAGCAGGGTG GAGACCGGAA GTCTTGTATT TGTTAACAAA AATGGGGACA 720
GCAGAGGGGG AAAAGCAGAG GGGAAGGGCC CCACGTCGGT CAGGGCCTTG CCCTCGCTCC 780
CTGCAGCCCC AGCTCCTCCT CTTGGGGACC TGGGGGGCAC AAAGCAGGGG TTGAGTGTGA 840
GATGTGTTTT GGTGTGGCCT TTGTGTTTCT GGAGTAACTG GGTTCAGAGT CAATGATGAT 900
GGGTTGCACC CTGCAGGGGG TCCATGGCGG AAGATGGGGC CGCATCCTGC TGCCCCAGCA 960
GGCTGGGTAA CTGGGGCAGC CCAGGACACT AACTGGCTCC AACTTTTACA GGCGTGTTAG 1020
GACCTGGGAA CCCACTGGCT CCACTCAGTT GTTGTTGTTG TTGTTGTTGT TTTAAGTAGC 1080
AGCCAGTGTT GGATGGAGGT GCCCGTCAGT AAGGCCATAC AAATGTGCAC ACTGCGGCCT 1140
GCTGGGGCAG CCACAGACAC ACACACCCAG AGCAGCGGTT CCCTACAGAC ACCCCAAGCT 1200
GGCCTTCCCA AATGCCTGCC CCAAAAGCTC CACAAAAAGG GGACACTGAG GTCTCATTCC 1260
TTTCCCTCAA CCCCCAACCC CCACTAAAAA TCAACACCAG AAAACTGGCC GGTCACCACC 1320
CCCCATGTAG CTTGGAAGTC CAGTGCTTGT GCATGTGCGT GTGCAAGACT GTGTCCATGA 1380
TGTCAGTGTG TACGAGTGTG TGTTATGTGT GTTTCTGTGT GCACATACGT ACTGGAACAT 1440
ATGGAAAACA AGACAGGGAC AGGGAGAAGG TGACTCATCA GGCATTCACT TGTTTCTGCA 1500
AAGTATCCAT CAACTGCTAA TAAACTTGTG AGCGCTGGCA ATCTTTGAAC TTTCTTGCTG 1560
AGGGAACTCA GCTCTGAAGG CTACACCAAA GACCTGAACG CCCAGGGAAG GAAGGACACA 1620
TTGGCATCAA GTGTGAAGCG GGGGAGAAAG CCCTCTTCCG GGAGGCACAG CACATCCACC 1680
CTTTTGGTGT GGAGGAGGGT GTTCTGAAAC ACAAGAAGCT TTTGCTTATT TTCCCAATTC 1740
GGGACAACAA ACCTGGCCTG GAAAGGAAGA CTCGAGGAGC TGCTGGGAAG GAGGCGGGAG 1800
GGAGGGTGGG TGGGAGACCC TCAGCAGAGC CTCACAATGC TTTGTTTCAT GCAGCCAGGA 1860
CCCACTGAAA CCTGGCACCG GCCAACAGGA GGAGGAGGAG GAGGAGCAAG GGAGTGAGTG 1920
GAGTATGGAC CTGAGATCGA GGTGCCCCCA TGCCAGGCCT GTCAGCCACC TAGGCAAGGG 1980
GTGGAAGCCT TGTCTGCCAA GGGTGGGGGC CTCTGGGGGC AGAGGAAGCT GGGTGGGGAC 2040
TGGAGCCTGA GATCTGTAGC AGGACGGGGA AGTGTCAGGT GGGTTTCTGT TTCATCTGTG 2100
CAGCCCGCCA GCAATGTGCT GCCAGACACC CCCTGGAAAA AGCATTTTTC TGCTGAGGTT 2160
AATGGCCCAG CCCAGAAAAA CTGCAATGCA TGGATGTCGT GAATGCTGCT GTGTGTGAAC 2220
AAGGGCCCTG AAGTCCATTT GGTGCCCTAA CCCACCGCAG GGAGACTCCT GCCTGCTCCT 2280
CCCTCGCTGT CCCCTCCAGC TCCCCCACCA GCAGCCTCTG TCCTCCCGTT AGGACAGCTC 2340
CAGTCTCCTC CTGCCGGGAC TATCTCTAAG CACACACAAA AAACAAGCTT TCCAGCAAAA 2400
CCATTCGGCA ACAGCAAAGG CCCCTCGAAC ACACACCCTT GTGTGGACAT CACACCTTCT 2460
GGGGACCCCG CACGACATCC CCCATTGCCA CTACAGAGAT TCCCCTTTGC CCTGAATTCC 2520
CCGCCATTTG GGCTCATTTC TGGGAAATGC TCAGCTTCAT CTTCACAGAA ACACAGTTCC 2580
CTGAATCGGG CCCACAGCCC ACACGAGTCT CCCCACAAAG GTCTGTGTGG ACGCTTTGCT 2640
CCCAGGGACT TCCCGGGCCA CGTGTCGAGG GGCTGGGAAG TTCAGTCAGT ACAAGGACTA 2700
AGGAAGAGCC TTGGCCTCTC GCTGATAGTT AACCTCTGAA GGCAAAACTC ACAGTCCTTT 2760
GTTAATTTCC CTCAGCTTTA TAACCTTTTC CGGTATTTTC CACAAACTTC TCCCCCTCCC 2820
CAGAAAACTG TACAGGGGCT TGTTTTAAAA CAGTATGTGT TCATTTTAAA GCATCCAAAA 2880
GAAAAGCTGT GTTGTAAAAA GCTCACTAAT CAGATGCCTG CTCACAGTTG TATCTTTTTA 2940
TTACAGTGTG GGGAATTTTT GGAGCAACAC CAGAAAAATG CTGAATCTGC CTAAAATTCC 3000
TTTAAGGTGT TGCCCCCCCC CAACCTTCCC CATTTCCCTT AAAGCATAAA ATCCTCCCTT 3060
TAAAGGGAAG GGGGAGGTGG GTGTTGAGAA AGGAGAGGAC TTCAGCCTGT GTTTGCGCTC 3120
CAACTGGGGA AGACCACTTA GCAAGGAGCT CCCTGACTCT TACAAAGAGT TATTTAATTA 3180
CCCTGCTCAT GAATGAACAG ACCAGACCCT TCCAGGAGAC CAGAGGCTCG TGAATGAACC 3240
TCACACCCCA GGTCTCAATG GCACAGGGTG ACCAGGCCTC AAGGCCACAT 3290