EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS129-05017 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr10:74051600-74054620 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7075993chr1074054590hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr10:74052950-74052961CCACACCCTGC+6.62
ZNF263MA0528.1chr10:74054051-74054072GCAGGAGGGAGAAGAGGAAGA+6.04
ZNF263MA0528.1chr10:74054048-74054069AAGGCAGGAGGGAGAAGAGGA+6.29
ZfxMA0146.2chr10:74051604-74051618TGGGCCCAGGCCTG+6.06
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_14408chr10:74052238-74053258CD4_Memory_Primary_7pool
SE_17857chr10:74053686-74059421CD4p_CD25-_CD45ROp_Memory
SE_19098chr10:74050446-74059564CD4p_CD25-_Il17-_PMAstim_Th
SE_19178chr10:74050502-74059546CD4p_CD25-_Il17p_PMAstim_Th17
SE_23522chr10:74052065-74052733Colon_Crypt_1
SE_24295chr10:74052122-74052656Colon_Crypt_2
SE_25357chr10:74051869-74053361DND41
SE_26542chr10:74051995-74053528Esophagus
SE_26542chr10:74053727-74056112Esophagus
SE_31487chr10:74052048-74053225Gastric
SE_32597chr10:74052076-74052841GM12878
SE_34068chr10:74051991-74053105HCC1954
SE_34255chr10:74050318-74054468HCT-116
SE_35862chr10:74051120-74053424HMEC
SE_35862chr10:74053514-74054850HMEC
SE_47212chr10:74051844-74053229Panc1
SE_47212chr10:74053450-74056305Panc1
SE_55105chr10:74052229-74052770Thymus
SE_55105chr10:74052835-74053287Thymus
SE_55794chr10:74053651-74054755u87
SE_57362chr10:74052113-74053348VACO_503
SE_59624chr10:74002380-74097763Ly4
SE_61087chr10:74002331-74097462HBL1
SE_61440chr10:74003751-74097541Toledo
SE_62229chr10:74002256-74105283Tonsil
SE_64442chr10:74051836-74053167NHEK
SE_65252chr10:74051162-74053813Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr107405284174053369
chr107405195274052573
chr107405197774052745
chr107405286274053338
chr107405367074054029
Number: 3             
IDChromosomeStartEnd
GH10I072291chr107405147274053359
GH10I072293chr107405355974054008
GH10I072294chr107405435474059383
Enhancer Sequence
TAGGTGGGCC CAGGCCTGCC TCTGTTTCCC CACCCTTCCC TGCCATAGAC TTGGTTAATC 60
AGCAGGTTGG GGAGGGGGAC CTGCTGCTCC CAGAGGCCGT AGGTGCTGGA GCACGAGGTA 120
AGAATGGCCA AGAGCTGGCT GGGCGCAGTG TCTCACGCCT GTAATCCCAG CACTTTGGGA 180
GGCCGAGGTG GGCAGATCAC CTGAGGTCGG GAGTTTGAGA CCAGCCTGAC CAACATGGAA 240
AAACCCCATC TCTGCTAAAA ATACAAAATT AGCCGGGAAT GGTGGCACAT GCCTGTAATC 300
CCAGCTACTC AGGAGGCTGA GGCAGGAGAA TCGCTTGAAC CCGAGTGGCG GAGGTTGCGG 360
TGAGCCGAGA TCATGCCTTT GGACTCCAGC CTGGGCAACA AGAGTAAGAC TCGGTCTAAA 420
AAAAGAAAAA AAAAGAATGG CCAAGAGCCA TCTTCTAGAA ATGGGGAGAA TGACTCAAAC 480
TGAATCAGGA GCAGGTGAGG TCACCCTGGG TACCTGGAGT TACTCAGAGT GACACTAGTA 540
CACGCCTGGC AGGAGTGATG GATGAGCTAG GCTCCAGGAA AGCAGGTGGG GCTGGAAACC 600
ACCCAAGACA AGGAAATTGT TGGGTTTGAA ATTCCAGGTA AGCAGAGTAT GGCCTGAGAG 660
CAGCGGCAGA GGCTGAAAGT GGGCTTGGTC TCGGTATTTT TGAGGCTGAG GTAGCTCCAA 720
CTCTCTCCCT CTGAGTCAGC ACCCCACTTA AGACAGAAAT ACTGAGATCT GCGACCCCAG 780
CCTCCCCCAC AGCAACTCCA CAGTCCCCAA ACCTTTGCTC CGCTGGGTCC TCCCAAGTAT 840
GGTAGCTGAC ACAGCCCTGA GCAGCCCACT GTCCTCTGCC CTGCCAAGTC TTCTCACTCT 900
TGTCACTTTG TCCTACATCA TTTCTTTGTC TGGCACCCCT CCTAGAATTG GTGCCCCAGA 960
GGTGGGAAAA ACCTACCCTG CTCACTGCTC TATCTCCTGG GCTTAGCTCA GACTCTGGCA 1020
TACGTGAGTG CTTAGTAGAA ACTTGATGGG GTATTAAAAT TGAGACCTGG GTGGGTTCTC 1080
ACATTAAATT TCTAACACTC CTTAGGTGGC TTGGGCCCAC CCCTCTGAGC CCTGTTTCCA 1140
CATCTGTAAA GTAGCAAACC ATCGCCATGA AGAACAGGGA AGAACCAGGT CAGCAGGCAG 1200
GGCGGATGAA GCATCCAGCC AGTTCTAGGA AGTTTCCGAT GGCTAATCCT TCAGATGCAG 1260
CTTGTAAGCA GGTCAAATAC AGAATAGGAA ACTGAGGCGC AACGAAGTCA TGCTTAGAAG 1320
TCTGTCCAGG GAGACCAGTC AAGGCCTCCC CCACACCCTG CAAGCCCTTC TAGGAGCTCT 1380
GGTTAAGTCA CTCTCGTTCA ATCTCCCTGA GAGGTACCAT CCACAGGTCC TGAAGTGTGT 1440
GGCCTGTCCC TGCTGTGTGA GGTGGCCCTC CCCATTCTGC TTCCTCTTTG AGGTGGCCTG 1500
GCTCCTGGTG GTAGGCAAGT GCTAGAAGAC AGCAGAGATG GCTGCCTCTG GTGTTGGGAG 1560
CTGGAGTCAA AGAGCCAGAG GGGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTAT 1620
GTTCATTATC CATAAGTACC CACTTGGCCC TCACTATACT CCAAGAGGGA GGCAGTCCAG 1680
CCTAGTGGTG AGATGGTGAG ATGCTCCCAC TATGGAGTCA GGCTGGAGTT GGCCTTGGGG 1740
CAGTCCTTCC TTTTTTTTTT TTTTTTTTTT TTTTTTTGAG ACGTAGTCTT GCTCTGTAGC 1800
CCAGGCTGGA GTGCAATGGC GTGATCTTGG CTCACTGCAA CCTCTGCCTC TCGGGTCCCG 1860
GTTCAAGCAA TTCTCCTGCC TCAGCCTCCC AAGTAGCTTG GACTACAGGC GCCCACCACC 1920
ACACCCAGCT AATTTTTGTA TTTTTAGTAG AGATGGGGTT TCACCATGTT GGCCAGGCTG 1980
GTCTCGAACT CCTGACCTCA GGTGATCTGC CCGCCTTGGC CTCCCAAAGT GCTGGGAGTA 2040
CAGGCCTGAG CCACCGCGCC CGGCCTGGGG CAGTCCTTCC TAAGCCCCAG TCTCCTACCT 2100
AAAAAAGATG GTTGTGAGGG TGTGGCATGC TCAGCACTCA GCACAGAGCC TTACTCACCA 2160
TTAACACTCA ACAAACAGCA TGTGTTGTTA GTTTTTGTTT TGAGACAGTC TCACTCTGTA 2220
GCCCAGGCTA GAGTGCAATC ATGGATCACT GCAGCCTTGA TCTCCTGGGC TCAAGTGATC 2280
CTCCCACCTC AGTCTCCCAA AGAGCTGGGA TTACAGGCAT AAGCCACCTT GCCCCGCCAG 2340
TTTTTAGCCT GTCAGCTCTT TGAGGGACAC TTGTTATGGT CATACCCACA GCTTTGACCC 2400
TTACCAGGTG GTCAGGTGGA TGAATGAATG AGTAGAAAGA AGGAAGAGAA GGCAGGAGGG 2460
AGAAGAGGAA GAATGAAGGA AGGGTTGAGT TTGTTCTGGA AGCTCCCAGC TTCCATCCGC 2520
ACCACACTCT CCCTCTGTCC CCAGGACACC AGGGAACTGA CTCAAGGCTC TCCTCTTACC 2580
AGGTGCTGTG TGGGGTCCAG GGAGAAGAGC CCATTTGAAA TGGGGCACTG GTCTAAACTC 2640
TGGACCTGCT GCTCACTATT GACTGAACTT AGCCACTTAA ATATTCTCCT CTATAAAATG 2700
GGAGTGACCA TAGCAACTAC CTCGCTGAAT TGTAGGGAGA CCCAAAAAAT GTATATGAAT 2760
ACATTTGTCA ACTAAAGAGT GTTAGGGATT ATCTCAGTGG AGGGATAGGC AGTGCAGGCT 2820
CTGGAACCAG ACTTCTTGTG TTCACATCCC TGCTCCACTG CTTGGAGACC TTTGGCAAGG 2880
TCCTTAACTC CTCTGGACCT CAGTTTTCTC ATCTGTAAAA CAGGGATTAT ACTAGTTCCT 2940
ACCTCACAGA GTTGTGAAGA TTAAATGAGA TAATGCATGA AAGGCTTTTC AATAAGAGCA 3000
GGGCACACAT TAGGCATGAT 3020