EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-33961 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr17:37909790-37912110 
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: 2             
ChromosomeStartEnd
chr173790980037910200
chr173791041137911394
Number: 1             
IDChromosomeStartEnd
GH17I039753chr173790929737916397
Enhancer Sequence
AGCGATTTTC CTGCCTCAGC CTCTTGAGTA GTTTGGGATT ACAGGCGTGC GCCACCACGC 60
CCAGCTAATT TTTGTATTTT TAGTAGACGG GGTTTTGCCA TGTTGGCCAG ACTGATCTCA 120
AACTCCTGAC CTCAAGTGAT CCTCCCGCTT TGGCCTCCCA AGGGAGGGTT CCTTCCTCCC 180
AGGCTGAGGC ACCCTGCCCC ACACATCTAC TGGAGGAACT TAGTGTTGGG GCCAGGGGGT 240
GGCTGGGTAA GGCTGGATCC CACACTTGTC AGGCCAGGTT GGGGTAGGGG AGGATACACG 300
GGGGACCCGT CTCTCAGCCG TTCTGGGCCG GTGCCTGAGG CGATCTGCCC CGCCGCCCGC 360
CCTTCCGCCA CCACCCAAGT CGCATGCGCG CGCCGGGGCC GACGGGCGCC AGGCTCCACC 420
GAGCCACCCT CCGTCGTGGC GGCCCCTCGT GCCTCTGCGG AGGGAAGGCC GCCGGCTTCG 480
CCAGGGGGCG CGCGTCGGGG TCGCGGCTCT TTGAACTCGG CCCCACGAGG GGACGCGCCA 540
TCGGTTTCGT GGCTTGCGTG GCGCCGCAGC AACGAGCCGG TCGCCCCGGG GCGTTGCTTA 600
GTCCGGGCCT CGCTGCGAGT CTGTGGGCGA GGCGGGAGGT GCTTCCTTGG CCAGGCGGGT 660
GGAGGAAGGT GTGGGCGCCG CATCCCAGCG TCGCGGAGCC TCCAGGCGCG GGCAGGCGAG 720
ACTGGCGTGC AGCGCGACGG CCTAGTCCCG GCGTCCCACC GTCCCCCACT CCCGCAGGCG 780
CCGAGCCGAT TCAGCCGCGC GGCTGCAGTG ACACCCAGCG GCCGTCGCGG GAAGTGCGGT 840
CGCCGCGGCC AGGCCTCCGG GGCTCCTGTC TCTCGAGGTT CCCACCCCGG TTACGCGCGG 900
GCACCCCGGA GGAGAGCGGC CGCGCGCTGC AGATGCCCGC GGGGGCACTT CCCCTGCCCC 960
TCCCCCGTTT CCTCCCCGCA GGCGCCCGAG CGCCGGGAGA TCCTGCGCAG CGGCAGTGCC 1020
CGGAAGGGCG GGGCGGGGTG CAGCAGCGGC GCTGGGCTGT GACCCGGGCA GTTTCACTTC 1080
TGGATCCTGC TCGGGCTGTG ATAGGACAGC GCGGGGGCAG CGGGGGAACA CGCGGGCACG 1140
CCGAGATCCG GCGCTCGGGA CCCCGATGAG GGGAGGCCTT TCACTCCTGG GGTGTCACGC 1200
GACCCACGCT TTCCTCCATG TCCACTCCCA CCCCCCATGG GTTCCACTTT GCTGTCCCCC 1260
GAGCTGCCGC TCCTCCCCAG CAGACACCGT CTCCGCCGGG GCTGCCGACC CCCGGAGAGG 1320
CCCCGAGCGG CGTGGGCGGC GGGAGGAGGG AGCTGTGAAG CCGCAGGCAG GGGGTTAGGC 1380
TGCGGGCTGC TGAGACGCCG AGCTGTTTCT CAGAAGTGCA GCTGCCCCTC CCCTCACACC 1440
CCCCTCACTC CCACCGCGCG CCGCACCCCT GCCCCCTCTC CGCCGGCCTC CCTTTCCTCT 1500
CCCAGGCACC CTAGCCGGGA ATCTGGGGTC TGGGTCCACG CAGAATTAAG AGGAGAACCT 1560
GAGAAAGGGC GGGGGCCGGG GGTTCAGACC CAGCCTCAGC GCGCGTTATT CCGAGCCTCC 1620
TATAATTCCA CAGGTGAGGG GATCCTGTCC CCTACCCCTG GGGTCCAGGA TTGGAATTTG 1680
ATAGAACAGT TAGGAAAATG ACATCTTGAG AGAGTCAGGG CCCGGCCACT ATTACTCTAG 1740
CTCCAGCGTC CAGTGAGGAG AGGAGAGAGA GGGAAGACCT GGAGCCCGGC TGGTGCAGTG 1800
AGGTTGAGGC CTGTCTTAGG AGTACCAGCT GGAAGGCCCT TCAGAGATCC CTGACTCTGG 1860
GGAAAATCAA CGCCCAGAAG GGGAAGTCAA GTGTCTGGGC TCATCCCGAG AGGGAGAGGG 1920
CTGGGATTGG AACCAGGACT CCAAATAGTT GCGGGAGTCT GCGACTGTCT TTTGCTTGGG 1980
ACTTCAGAGC TTTGCTGGAT TCACTGACTC AGCCTGCTTT CCCTCAACAC ACACAAACAC 2040
ACACACACGA GACACGTGCA CGCGCGCACA CACACAGATA CACAGACACA CACAGACAGA 2100
CATGCAAGGA GAGAGACAGG CACACATGGA GACAGACACG CACACGCAAA GAGACACACA 2160
GCTCCCCAGG AGTCTAGCGG GGCAGCTGAG GTCTGTGAGT GAGACATTCT CAGTGAGACA 2220
CTGAGAATGC AATTCCAGTG GGGGTGGGAT GGGGATTGGG CGGTGGAAGG ACAAGCCCGG 2280
GGGAGGAGGT GGCATCGCCC CCCTAGTTCC CATCCACCAC 2320