EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-14728 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr17:37909860-37912010 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2941522chr1737910368hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr17:37911206-37911219TGCAGCTGCCCCT+6.22
TFAP2AMA0003.3chr17:37910121-37910132TGCCTGAGGCG-6.62
ZNF263MA0528.1chr17:37911543-37911564TGAGGAGAGGAGAGAGAGGGA+6.06
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_10214chr17:37909224-37910777CD19_Primary
SE_10214chr17:37910780-37916505CD19_Primary
SE_10853chr17:37908831-37940013CD20
SE_11904chr17:37909311-37910613CD3
SE_11904chr17:37910792-37913737CD3
SE_14700chr17:37909278-37913385CD4_Memory_Primary_7pool
SE_15787chr17:37909511-37913218CD4_Memory_Primary_8pool
SE_16504chr17:37909204-37913320CD4_Naive_Primary_8pool
SE_17008chr17:37909810-37915266CD4p_CD225int_CD127p_Tmem
SE_17573chr17:37908953-37916175CD4p_CD25-_CD45RAp_Naive
SE_17896chr17:37909110-37915660CD4p_CD25-_CD45ROp_Memory
SE_18319chr17:37909158-37916527CD4p_CD25-_Il17-_PMAstim_Th
SE_19193chr17:37909271-37915605CD4p_CD25-_Il17p_PMAstim_Th17
SE_20202chr17:37909188-37916568CD56
SE_21224chr17:37909428-37913178CD8_Memory_7pool
SE_22122chr17:37909402-37915298CD8_Naive_8pool
SE_22381chr17:37908953-37916600CD8_primiary
SE_24275chr17:37909791-37912087Colon_Crypt_2
SE_25150chr17:37909728-37911614Colon_Crypt_3
SE_31091chr17:37909377-37915449Fetal_Thymus
SE_32555chr17:37909259-37916398GM12878
SE_33366chr17:37910098-37910578H1
SE_43567chr17:37909660-37915502MM1S
SE_47831chr17:37909909-37911257Pancreas
SE_50466chr17:37909230-37915264Sigmoid_Colon
SE_52845chr17:37909201-37915243Small_Intestine
SE_54478chr17:37909533-37913988Spleen
SE_55194chr17:37909333-37915072Thymus
SE_56927chr17:37909754-37911992VACO_400
SE_57786chr17:37909864-37911513VACO_503
SE_58042chr17:37909910-37911340VACO_9m
SE_58368chr17:37909481-37978016Ly1
SE_58889chr17:37909243-37979334Ly3
SE_60123chr17:37909329-37924165Ly4
SE_60580chr17:37909490-37957939DHL6
SE_60998chr17:37907678-37978969HBL1
SE_62252chr17:37909189-37978818Tonsil
SE_65636chr17:37909344-37912457Pancreatic_islets
SE_67296chr17:37909660-37915502MM1S
SE_69015chr17:37909810-37911434H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr173791041137911394
Number: 1             
IDChromosomeStartEnd
GH17I039753chr173790929737916397
Enhancer Sequence
TTTGTATTTT TAGTAGACGG GGTTTTGCCA TGTTGGCCAG ACTGATCTCA AACTCCTGAC 60
CTCAAGTGAT CCTCCCGCTT TGGCCTCCCA AGGGAGGGTT CCTTCCTCCC AGGCTGAGGC 120
ACCCTGCCCC ACACATCTAC TGGAGGAACT TAGTGTTGGG GCCAGGGGGT GGCTGGGTAA 180
GGCTGGATCC CACACTTGTC AGGCCAGGTT GGGGTAGGGG AGGATACACG GGGGACCCGT 240
CTCTCAGCCG TTCTGGGCCG GTGCCTGAGG CGATCTGCCC CGCCGCCCGC CCTTCCGCCA 300
CCACCCAAGT CGCATGCGCG CGCCGGGGCC GACGGGCGCC AGGCTCCACC GAGCCACCCT 360
CCGTCGTGGC GGCCCCTCGT GCCTCTGCGG AGGGAAGGCC GCCGGCTTCG CCAGGGGGCG 420
CGCGTCGGGG TCGCGGCTCT TTGAACTCGG CCCCACGAGG GGACGCGCCA TCGGTTTCGT 480
GGCTTGCGTG GCGCCGCAGC AACGAGCCGG TCGCCCCGGG GCGTTGCTTA GTCCGGGCCT 540
CGCTGCGAGT CTGTGGGCGA GGCGGGAGGT GCTTCCTTGG CCAGGCGGGT GGAGGAAGGT 600
GTGGGCGCCG CATCCCAGCG TCGCGGAGCC TCCAGGCGCG GGCAGGCGAG ACTGGCGTGC 660
AGCGCGACGG CCTAGTCCCG GCGTCCCACC GTCCCCCACT CCCGCAGGCG CCGAGCCGAT 720
TCAGCCGCGC GGCTGCAGTG ACACCCAGCG GCCGTCGCGG GAAGTGCGGT CGCCGCGGCC 780
AGGCCTCCGG GGCTCCTGTC TCTCGAGGTT CCCACCCCGG TTACGCGCGG GCACCCCGGA 840
GGAGAGCGGC CGCGCGCTGC AGATGCCCGC GGGGGCACTT CCCCTGCCCC TCCCCCGTTT 900
CCTCCCCGCA GGCGCCCGAG CGCCGGGAGA TCCTGCGCAG CGGCAGTGCC CGGAAGGGCG 960
GGGCGGGGTG CAGCAGCGGC GCTGGGCTGT GACCCGGGCA GTTTCACTTC TGGATCCTGC 1020
TCGGGCTGTG ATAGGACAGC GCGGGGGCAG CGGGGGAACA CGCGGGCACG CCGAGATCCG 1080
GCGCTCGGGA CCCCGATGAG GGGAGGCCTT TCACTCCTGG GGTGTCACGC GACCCACGCT 1140
TTCCTCCATG TCCACTCCCA CCCCCCATGG GTTCCACTTT GCTGTCCCCC GAGCTGCCGC 1200
TCCTCCCCAG CAGACACCGT CTCCGCCGGG GCTGCCGACC CCCGGAGAGG CCCCGAGCGG 1260
CGTGGGCGGC GGGAGGAGGG AGCTGTGAAG CCGCAGGCAG GGGGTTAGGC TGCGGGCTGC 1320
TGAGACGCCG AGCTGTTTCT CAGAAGTGCA GCTGCCCCTC CCCTCACACC CCCCTCACTC 1380
CCACCGCGCG CCGCACCCCT GCCCCCTCTC CGCCGGCCTC CCTTTCCTCT CCCAGGCACC 1440
CTAGCCGGGA ATCTGGGGTC TGGGTCCACG CAGAATTAAG AGGAGAACCT GAGAAAGGGC 1500
GGGGGCCGGG GGTTCAGACC CAGCCTCAGC GCGCGTTATT CCGAGCCTCC TATAATTCCA 1560
CAGGTGAGGG GATCCTGTCC CCTACCCCTG GGGTCCAGGA TTGGAATTTG ATAGAACAGT 1620
TAGGAAAATG ACATCTTGAG AGAGTCAGGG CCCGGCCACT ATTACTCTAG CTCCAGCGTC 1680
CAGTGAGGAG AGGAGAGAGA GGGAAGACCT GGAGCCCGGC TGGTGCAGTG AGGTTGAGGC 1740
CTGTCTTAGG AGTACCAGCT GGAAGGCCCT TCAGAGATCC CTGACTCTGG GGAAAATCAA 1800
CGCCCAGAAG GGGAAGTCAA GTGTCTGGGC TCATCCCGAG AGGGAGAGGG CTGGGATTGG 1860
AACCAGGACT CCAAATAGTT GCGGGAGTCT GCGACTGTCT TTTGCTTGGG ACTTCAGAGC 1920
TTTGCTGGAT TCACTGACTC AGCCTGCTTT CCCTCAACAC ACACAAACAC ACACACACGA 1980
GACACGTGCA CGCGCGCACA CACACAGATA CACAGACACA CACAGACAGA CATGCAAGGA 2040
GAGAGACAGG CACACATGGA GACAGACACG CACACGCAAA GAGACACACA GCTCCCCAGG 2100
AGTCTAGCGG GGCAGCTGAG GTCTGTGAGT GAGACATTCT CAGTGAGACA 2150