EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS139-22945 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr17:37909870-37911530 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2941522chr1737910368hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr17:37911206-37911219TGCAGCTGCCCCT+6.22
TFAP2AMA0003.3chr17:37910121-37910132TGCCTGAGGCG-6.62
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
TAGTAGACGG GGTTTTGCCA TGTTGGCCAG ACTGATCTCA AACTCCTGAC CTCAAGTGAT 60
CCTCCCGCTT TGGCCTCCCA AGGGAGGGTT CCTTCCTCCC AGGCTGAGGC ACCCTGCCCC 120
ACACATCTAC TGGAGGAACT TAGTGTTGGG GCCAGGGGGT GGCTGGGTAA GGCTGGATCC 180
CACACTTGTC AGGCCAGGTT GGGGTAGGGG AGGATACACG GGGGACCCGT CTCTCAGCCG 240
TTCTGGGCCG GTGCCTGAGG CGATCTGCCC CGCCGCCCGC CCTTCCGCCA CCACCCAAGT 300
CGCATGCGCG CGCCGGGGCC GACGGGCGCC AGGCTCCACC GAGCCACCCT CCGTCGTGGC 360
GGCCCCTCGT GCCTCTGCGG AGGGAAGGCC GCCGGCTTCG CCAGGGGGCG CGCGTCGGGG 420
TCGCGGCTCT TTGAACTCGG CCCCACGAGG GGACGCGCCA TCGGTTTCGT GGCTTGCGTG 480
GCGCCGCAGC AACGAGCCGG TCGCCCCGGG GCGTTGCTTA GTCCGGGCCT CGCTGCGAGT 540
CTGTGGGCGA GGCGGGAGGT GCTTCCTTGG CCAGGCGGGT GGAGGAAGGT GTGGGCGCCG 600
CATCCCAGCG TCGCGGAGCC TCCAGGCGCG GGCAGGCGAG ACTGGCGTGC AGCGCGACGG 660
CCTAGTCCCG GCGTCCCACC GTCCCCCACT CCCGCAGGCG CCGAGCCGAT TCAGCCGCGC 720
GGCTGCAGTG ACACCCAGCG GCCGTCGCGG GAAGTGCGGT CGCCGCGGCC AGGCCTCCGG 780
GGCTCCTGTC TCTCGAGGTT CCCACCCCGG TTACGCGCGG GCACCCCGGA GGAGAGCGGC 840
CGCGCGCTGC AGATGCCCGC GGGGGCACTT CCCCTGCCCC TCCCCCGTTT CCTCCCCGCA 900
GGCGCCCGAG CGCCGGGAGA TCCTGCGCAG CGGCAGTGCC CGGAAGGGCG GGGCGGGGTG 960
CAGCAGCGGC GCTGGGCTGT GACCCGGGCA GTTTCACTTC TGGATCCTGC TCGGGCTGTG 1020
ATAGGACAGC GCGGGGGCAG CGGGGGAACA CGCGGGCACG CCGAGATCCG GCGCTCGGGA 1080
CCCCGATGAG GGGAGGCCTT TCACTCCTGG GGTGTCACGC GACCCACGCT TTCCTCCATG 1140
TCCACTCCCA CCCCCCATGG GTTCCACTTT GCTGTCCCCC GAGCTGCCGC TCCTCCCCAG 1200
CAGACACCGT CTCCGCCGGG GCTGCCGACC CCCGGAGAGG CCCCGAGCGG CGTGGGCGGC 1260
GGGAGGAGGG AGCTGTGAAG CCGCAGGCAG GGGGTTAGGC TGCGGGCTGC TGAGACGCCG 1320
AGCTGTTTCT CAGAAGTGCA GCTGCCCCTC CCCTCACACC CCCCTCACTC CCACCGCGCG 1380
CCGCACCCCT GCCCCCTCTC CGCCGGCCTC CCTTTCCTCT CCCAGGCACC CTAGCCGGGA 1440
ATCTGGGGTC TGGGTCCACG CAGAATTAAG AGGAGAACCT GAGAAAGGGC GGGGGCCGGG 1500
GGTTCAGACC CAGCCTCAGC GCGCGTTATT CCGAGCCTCC TATAATTCCA CAGGTGAGGG 1560
GATCCTGTCC CCTACCCCTG GGGTCCAGGA TTGGAATTTG ATAGAACAGT TAGGAAAATG 1620
ACATCTTGAG AGAGTCAGGG CCCGGCCACT ATTACTCTAG 1660