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

TagContent
EnhancerAtlas ID
HS087-00191 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr1:8467580-8470000 
SNPs
Number: 1             
IDChromosomePositionGenome Version
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: 1             
ChromosomeStartEnd
chr184678248468935
Number: 1             
IDChromosomeStartEnd
GH01I008406chr184664498473883
Enhancer Sequence
ACTTGCAACA GAAGCTCTGT GGGGGAAGCC TACCTCTCAA GGCCCTAGTT CTTGGCTCAT 60
CCCCACCCCA TGACCTGGAC AAGACCTGTG AGGGTGCCAT TTTTAGTATC ACCGTGCCTC 120
AGTTTCTCCA CCTGTGCATG TGGAATGATA CTGGCAGCCC CCGTAGACTT ATGGGGATGA 180
CTGCTGAGCT GATGTCTATA AAATGTTCTT AATGGCAAGG GCGAAAGAGC TATAAATACA 240
AGGTCAAAGC AGCATTTAAA ACCTTTTTAA AGCTGCAGCC ACTTCTTTCT TTTGAAACAG 300
AGAACCACAG GGAGGATCAA AGGCGTGCTG CTGTTAACTG CGGCTCTCAA GGCCTTGCCC 360
TCCACCTGGC AGAAACCCTA GAGAGGTCTA CCATGATTTT TACCTTGACT AACAAAATCT 420
CAAGACAAGT TGTACAATGG TTTCCTGGAA CATTCTGAGT AAAGAAATGG GAAACCAATA 480
CAGCTTACCT AGCTTGTTAC CTTCTATGAA CGCTGGCATT AAAAGTAAAA GGCAGCCTTG 540
GGAGGAAGAA ATGCAAACAC AGAGGGAGAA CATAGCTTCC CCTTGTCTCT CTCTGCCACA 600
AAAGCCTGGC CAAAGTGACT CTACTAGGTT GAAGCAGCCT GCATAATAAA ACGCTTAACC 660
TTGGCTAAGT TAACCTCCTC AGCCATTAAA AAAAGGGAGG GTGGGGGAAG GGCTAGCAAA 720
ATCAAGCTTA CGGGAAATAA ACCTAATCAA AGCCGAGTAG TAACAAAGGG CACCAGAAAC 780
ATTTCTACTG TATCACATCC CACAGGCTGG CCAAGAGCCC GGAATTTTCA TTACAACTTT 840
CAAAGAGAGC AAGAGGAGGA GGGAAAAAGA TTTCACAAAA GCATTATCAA GGCCCCAACC 900
CAGGATGCCC TGCTGTACAA CCAAAATTTG TAAGAGGTCA GCCTTTCAGG GAGTCAAAAA 960
CCCAGCATGT GGAAACTGGC AGGCCTTTTA TATAGTGGGA GGGGTTCTTA AAACGACTAC 1020
TGTTTCGCAC TGAAGTCTCT GAGCTTCACA GATCATTAAA GGTTTCTGAA CCACAGAGAA 1080
AGGAGGGCAG AGTTAAGGAA ATAAATCAAA AGTTCCTCTG GGACGCACAA ATGCCTACTT 1140
GGAACAGGCT TTCAGCATGA ATATCCTCCA CATTAAACAA CAGGGAGGAC TTTTCAAAAT 1200
AAAAGCAGAA AAGAGATTCA TTTTGTTACA AGCAATGCAC TTTTTCCTTT TGGTGTAAAG 1260
GTTATGTGTG CTATAAAAAA TGACTCCTGC CGTGAGTGCT GCGGGGAGGT GGAGGCTGGG 1320
CTTGGGGCAG GAGGTGGTGG TGGTCAAAGA AAACAAGTAG AAGTGAATAC AACGCCTGAG 1380
AATGCTGTGT TTGGGGGTCC CCCAAACAAG TCTAAATGTC CCGCAATGAT TTGGGGGTAG 1440
GATGTGAGGT AGGAGAATGG TATCAGAAAG GAATTTCTTC TACATTTATT CCTTGCCATC 1500
CTTGCCCAAG AACTGAAATC ATTTCCCCAC AGCCAGAAAG AACTGTCTTC TTTGTGGGTG 1560
TGCAACACAC ACAGTTGCAG ATCTGGGGAA AAGAGACTGT GCCGTTTTGA AGGCAGAGCC 1620
TCACACTTCT TAAGGAAATA TCAGTTGTCT CAAAACCAGC AGAGGGAGTA CAACGTTTGA 1680
GAAGAGGAAT GGCCAACCCG ATTGCTGAGG ATTCATGTTT AGCCCCGACA ATGGTTGTAA 1740
AGCTGAGCTA TCTACCATAA CTTCTGCCCT TGCTCTCCTG TCACCCAGCA ATAGTAAACA 1800
GAAAGAAAAG CTATACTACC TACTCAGATG GAATTAGCTT GTTCTAACAA CCGCATGAGG 1860
CAGCAGAGAG AAAAGGAGAA CTGTCCACAC TTCTGTCGGG ACACAGTTCC TGTGAGCAGC 1920
ACTGTTTTGG GGAGAGGAAT AGAAGCAGGG GGAAGGCTCA ATGAAAAGCA GAAAGTCCAA 1980
TTTGGACTGA CAGCAAATCC CAAAGCAATG ATTTTACCTT AAAATCCAGG GCTCCTAGGC 2040
CAGTCTGTGA ACAGCTCATT TCCAGAATTT TTGTTTATGA GAGGGCAAAA TGGAGAACTC 2100
TGTCTTTCAA GCTTTTCTTT CAACAGATGA TTTGAAACAA AAGCAGCACA CTCATGAAGG 2160
CGTATGTCTG CTAAATGGTT GCTATCTTAA TCTTTAGCCA CAGTTTATCA AAACATGTAG 2220
GAATGGGTTG AGAAATTAAC TGGTGCTAAG ATTATCAGCA TGGACAAGTT CCTGGGGAGG 2280
GCCTGGCGAC ATGATCAAAG CTAATGGTCC CTCTCCCAGG AGCAAAGAGC CTACTATTTC 2340
ATGCATGATG ATGTTGGGCT CTGGCACTGG AAATCTTTGC TCAGGTCCAT TCTAAGTGTC 2400
GAAATGGTGT AATTAATGGT 2420