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

TagContent
EnhancerAtlas ID
HS051-00099 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr1:8467510-8470030 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs301793chr18467534hg19
rs2661868chr18469789hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr1:8468425-8468446AGAGCAAGAGGAGGAGGGAAA+6.37
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00045chr1:8465614-8485937Adipose_Nuclei
SE_02022chr1:8466991-8471024Aorta
SE_02685chr1:8467735-8469964Astrocytes
SE_03407chr1:8467813-8468400Brain_Angular_Gyrus
SE_03407chr1:8468677-8470010Brain_Angular_Gyrus
SE_03947chr1:8466807-8473327Brain_Anterior_Caudate
SE_04978chr1:8466924-8470167Brain_Cingulate_Gyrus
SE_06073chr1:8466667-8470657Brain_Hippocampus_Middle
SE_07042chr1:8466701-8471358Brain_Hippocampus_Middle_150
SE_07921chr1:8466804-8471472Brain_Inferior_Temporal_Lobe
SE_11329chr1:8466472-8473455CD20
SE_18764chr1:8466923-8470198CD4p_CD25-_Il17-_PMAstim_Th
SE_23717chr1:8466974-8470485Colon_Crypt_1
SE_25808chr1:8466353-8473444Duodenum_Smooth_Muscle
SE_27457chr1:8466851-8470528Esophagus
SE_28078chr1:8467183-8470904Fetal_Intestine
SE_29095chr1:8467196-8473478Fetal_Intestine_Large
SE_29887chr1:8467449-8470059Fetal_Muscle
SE_31622chr1:8466865-8470596Gastric
SE_37218chr1:8466239-8470256HSMMtube
SE_39132chr1:8466683-8471809IMR90
SE_40658chr1:8466715-8471128Left_Ventricle
SE_41679chr1:8466919-8468466LNCaP
SE_41679chr1:8468658-8470018LNCaP
SE_42166chr1:8466945-8470070Lung
SE_44612chr1:8466766-8473359NHDF-Ad
SE_45170chr1:8466866-8470172NHLF
SE_45677chr1:8466378-8473709Osteoblasts
SE_47251chr1:8465934-8485673Panc1
SE_48103chr1:8466858-8473292Psoas_Muscle
SE_48600chr1:8466803-8471085Right_Atrium
SE_50481chr1:8466781-8471143Sigmoid_Colon
SE_51176chr1:8466318-8473509Skeletal_Muscle
SE_52016chr1:8467848-8469979Skeletal_Muscle_Myoblast
SE_52725chr1:8466891-8471022Small_Intestine
SE_53408chr1:8466735-8470786Spleen
SE_54752chr1:8466519-8470951Stomach_Smooth_Muscle
SE_58576chr1:8455425-8501956Ly1
SE_60758chr1:8454848-8500160DHL6
SE_62661chr1:8450826-8509851Tonsil
SE_63725chr1:8467763-8470039HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr184678248468935
chr184689498470010
Number: 1             
IDChromosomeStartEnd
GH01I008406chr184664498473883
Enhancer Sequence
AAGAATGTCT AAGATAATAA AATTCCACTT TTTTTTTCTA TAAAAAGCAA ATCTTGTCCC 60
AGATGCAAGC ACTTGCAACA GAAGCTCTGT GGGGGAAGCC TACCTCTCAA GGCCCTAGTT 120
CTTGGCTCAT CCCCACCCCA TGACCTGGAC AAGACCTGTG AGGGTGCCAT TTTTAGTATC 180
ACCGTGCCTC AGTTTCTCCA CCTGTGCATG TGGAATGATA CTGGCAGCCC CCGTAGACTT 240
ATGGGGATGA CTGCTGAGCT GATGTCTATA AAATGTTCTT AATGGCAAGG GCGAAAGAGC 300
TATAAATACA AGGTCAAAGC AGCATTTAAA ACCTTTTTAA AGCTGCAGCC ACTTCTTTCT 360
TTTGAAACAG AGAACCACAG GGAGGATCAA AGGCGTGCTG CTGTTAACTG CGGCTCTCAA 420
GGCCTTGCCC TCCACCTGGC AGAAACCCTA GAGAGGTCTA CCATGATTTT TACCTTGACT 480
AACAAAATCT CAAGACAAGT TGTACAATGG TTTCCTGGAA CATTCTGAGT AAAGAAATGG 540
GAAACCAATA CAGCTTACCT AGCTTGTTAC CTTCTATGAA CGCTGGCATT AAAAGTAAAA 600
GGCAGCCTTG GGAGGAAGAA ATGCAAACAC AGAGGGAGAA CATAGCTTCC CCTTGTCTCT 660
CTCTGCCACA AAAGCCTGGC CAAAGTGACT CTACTAGGTT GAAGCAGCCT GCATAATAAA 720
ACGCTTAACC TTGGCTAAGT TAACCTCCTC AGCCATTAAA AAAAGGGAGG GTGGGGGAAG 780
GGCTAGCAAA ATCAAGCTTA CGGGAAATAA ACCTAATCAA AGCCGAGTAG TAACAAAGGG 840
CACCAGAAAC ATTTCTACTG TATCACATCC CACAGGCTGG CCAAGAGCCC GGAATTTTCA 900
TTACAACTTT CAAAGAGAGC AAGAGGAGGA GGGAAAAAGA TTTCACAAAA GCATTATCAA 960
GGCCCCAACC CAGGATGCCC TGCTGTACAA CCAAAATTTG TAAGAGGTCA GCCTTTCAGG 1020
GAGTCAAAAA CCCAGCATGT GGAAACTGGC AGGCCTTTTA TATAGTGGGA GGGGTTCTTA 1080
AAACGACTAC TGTTTCGCAC TGAAGTCTCT GAGCTTCACA GATCATTAAA GGTTTCTGAA 1140
CCACAGAGAA AGGAGGGCAG AGTTAAGGAA ATAAATCAAA AGTTCCTCTG GGACGCACAA 1200
ATGCCTACTT GGAACAGGCT TTCAGCATGA ATATCCTCCA CATTAAACAA CAGGGAGGAC 1260
TTTTCAAAAT AAAAGCAGAA AAGAGATTCA TTTTGTTACA AGCAATGCAC TTTTTCCTTT 1320
TGGTGTAAAG GTTATGTGTG CTATAAAAAA TGACTCCTGC CGTGAGTGCT GCGGGGAGGT 1380
GGAGGCTGGG CTTGGGGCAG GAGGTGGTGG TGGTCAAAGA AAACAAGTAG AAGTGAATAC 1440
AACGCCTGAG AATGCTGTGT TTGGGGGTCC CCCAAACAAG TCTAAATGTC CCGCAATGAT 1500
TTGGGGGTAG GATGTGAGGT AGGAGAATGG TATCAGAAAG GAATTTCTTC TACATTTATT 1560
CCTTGCCATC CTTGCCCAAG AACTGAAATC ATTTCCCCAC AGCCAGAAAG AACTGTCTTC 1620
TTTGTGGGTG TGCAACACAC ACAGTTGCAG ATCTGGGGAA AAGAGACTGT GCCGTTTTGA 1680
AGGCAGAGCC TCACACTTCT TAAGGAAATA TCAGTTGTCT CAAAACCAGC AGAGGGAGTA 1740
CAACGTTTGA GAAGAGGAAT GGCCAACCCG ATTGCTGAGG ATTCATGTTT AGCCCCGACA 1800
ATGGTTGTAA AGCTGAGCTA TCTACCATAA CTTCTGCCCT TGCTCTCCTG TCACCCAGCA 1860
ATAGTAAACA GAAAGAAAAG CTATACTACC TACTCAGATG GAATTAGCTT GTTCTAACAA 1920
CCGCATGAGG CAGCAGAGAG AAAAGGAGAA CTGTCCACAC TTCTGTCGGG ACACAGTTCC 1980
TGTGAGCAGC ACTGTTTTGG GGAGAGGAAT AGAAGCAGGG GGAAGGCTCA ATGAAAAGCA 2040
GAAAGTCCAA TTTGGACTGA CAGCAAATCC CAAAGCAATG ATTTTACCTT AAAATCCAGG 2100
GCTCCTAGGC CAGTCTGTGA ACAGCTCATT TCCAGAATTT TTGTTTATGA GAGGGCAAAA 2160
TGGAGAACTC TGTCTTTCAA GCTTTTCTTT CAACAGATGA TTTGAAACAA AAGCAGCACA 2220
CTCATGAAGG CGTATGTCTG CTAAATGGTT GCTATCTTAA TCTTTAGCCA CAGTTTATCA 2280
AAACATGTAG GAATGGGTTG AGAAATTAAC TGGTGCTAAG ATTATCAGCA TGGACAAGTT 2340
CCTGGGGAGG GCCTGGCGAC ATGATCAAAG CTAATGGTCC CTCTCCCAGG AGCAAAGAGC 2400
CTACTATTTC ATGCATGATG ATGTTGGGCT CTGGCACTGG AAATCTTTGC TCAGGTCCAT 2460
TCTAAGTGTC GAAATGGTGT AATTAATGGT TAGCCTGGGT ATGCACTATT CAATCAGGCA 2520