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

TagContent
EnhancerAtlas ID
HS098-00283 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr1:8467660-8470030 
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: 2             
ChromosomeStartEnd
chr184678248468935
chr184689498470010
Number: 1             
IDChromosomeStartEnd
GH01I008406chr184664498473883
Enhancer Sequence
AAGACCTGTG AGGGTGCCAT TTTTAGTATC ACCGTGCCTC AGTTTCTCCA CCTGTGCATG 60
TGGAATGATA CTGGCAGCCC CCGTAGACTT ATGGGGATGA CTGCTGAGCT GATGTCTATA 120
AAATGTTCTT AATGGCAAGG GCGAAAGAGC TATAAATACA AGGTCAAAGC AGCATTTAAA 180
ACCTTTTTAA AGCTGCAGCC ACTTCTTTCT TTTGAAACAG AGAACCACAG GGAGGATCAA 240
AGGCGTGCTG CTGTTAACTG CGGCTCTCAA GGCCTTGCCC TCCACCTGGC AGAAACCCTA 300
GAGAGGTCTA CCATGATTTT TACCTTGACT AACAAAATCT CAAGACAAGT TGTACAATGG 360
TTTCCTGGAA CATTCTGAGT AAAGAAATGG GAAACCAATA CAGCTTACCT AGCTTGTTAC 420
CTTCTATGAA CGCTGGCATT AAAAGTAAAA GGCAGCCTTG GGAGGAAGAA ATGCAAACAC 480
AGAGGGAGAA CATAGCTTCC CCTTGTCTCT CTCTGCCACA AAAGCCTGGC CAAAGTGACT 540
CTACTAGGTT GAAGCAGCCT GCATAATAAA ACGCTTAACC TTGGCTAAGT TAACCTCCTC 600
AGCCATTAAA AAAAGGGAGG GTGGGGGAAG GGCTAGCAAA ATCAAGCTTA CGGGAAATAA 660
ACCTAATCAA AGCCGAGTAG TAACAAAGGG CACCAGAAAC ATTTCTACTG TATCACATCC 720
CACAGGCTGG CCAAGAGCCC GGAATTTTCA TTACAACTTT CAAAGAGAGC AAGAGGAGGA 780
GGGAAAAAGA TTTCACAAAA GCATTATCAA GGCCCCAACC CAGGATGCCC TGCTGTACAA 840
CCAAAATTTG TAAGAGGTCA GCCTTTCAGG GAGTCAAAAA CCCAGCATGT GGAAACTGGC 900
AGGCCTTTTA TATAGTGGGA GGGGTTCTTA AAACGACTAC TGTTTCGCAC TGAAGTCTCT 960
GAGCTTCACA GATCATTAAA GGTTTCTGAA CCACAGAGAA AGGAGGGCAG AGTTAAGGAA 1020
ATAAATCAAA AGTTCCTCTG GGACGCACAA ATGCCTACTT GGAACAGGCT TTCAGCATGA 1080
ATATCCTCCA CATTAAACAA CAGGGAGGAC TTTTCAAAAT AAAAGCAGAA AAGAGATTCA 1140
TTTTGTTACA AGCAATGCAC TTTTTCCTTT TGGTGTAAAG GTTATGTGTG CTATAAAAAA 1200
TGACTCCTGC CGTGAGTGCT GCGGGGAGGT GGAGGCTGGG CTTGGGGCAG GAGGTGGTGG 1260
TGGTCAAAGA AAACAAGTAG AAGTGAATAC AACGCCTGAG AATGCTGTGT TTGGGGGTCC 1320
CCCAAACAAG TCTAAATGTC CCGCAATGAT TTGGGGGTAG GATGTGAGGT AGGAGAATGG 1380
TATCAGAAAG GAATTTCTTC TACATTTATT CCTTGCCATC CTTGCCCAAG AACTGAAATC 1440
ATTTCCCCAC AGCCAGAAAG AACTGTCTTC TTTGTGGGTG TGCAACACAC ACAGTTGCAG 1500
ATCTGGGGAA AAGAGACTGT GCCGTTTTGA AGGCAGAGCC TCACACTTCT TAAGGAAATA 1560
TCAGTTGTCT CAAAACCAGC AGAGGGAGTA CAACGTTTGA GAAGAGGAAT GGCCAACCCG 1620
ATTGCTGAGG ATTCATGTTT AGCCCCGACA ATGGTTGTAA AGCTGAGCTA TCTACCATAA 1680
CTTCTGCCCT TGCTCTCCTG TCACCCAGCA ATAGTAAACA GAAAGAAAAG CTATACTACC 1740
TACTCAGATG GAATTAGCTT GTTCTAACAA CCGCATGAGG CAGCAGAGAG AAAAGGAGAA 1800
CTGTCCACAC TTCTGTCGGG ACACAGTTCC TGTGAGCAGC ACTGTTTTGG GGAGAGGAAT 1860
AGAAGCAGGG GGAAGGCTCA ATGAAAAGCA GAAAGTCCAA TTTGGACTGA CAGCAAATCC 1920
CAAAGCAATG ATTTTACCTT AAAATCCAGG GCTCCTAGGC CAGTCTGTGA ACAGCTCATT 1980
TCCAGAATTT TTGTTTATGA GAGGGCAAAA TGGAGAACTC TGTCTTTCAA GCTTTTCTTT 2040
CAACAGATGA TTTGAAACAA AAGCAGCACA CTCATGAAGG CGTATGTCTG CTAAATGGTT 2100
GCTATCTTAA TCTTTAGCCA CAGTTTATCA AAACATGTAG GAATGGGTTG AGAAATTAAC 2160
TGGTGCTAAG ATTATCAGCA TGGACAAGTT CCTGGGGAGG GCCTGGCGAC ATGATCAAAG 2220
CTAATGGTCC CTCTCCCAGG AGCAAAGAGC CTACTATTTC ATGCATGATG ATGTTGGGCT 2280
CTGGCACTGG AAATCTTTGC TCAGGTCCAT TCTAAGTGTC GAAATGGTGT AATTAATGGT 2340
TAGCCTGGGT ATGCACTATT CAATCAGGCA 2370