EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS094-43984 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr9:134582090-134584410 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXC1MA0032.2chr9:134582464-134582475TAAGTAAACAT+6.02
HNF4GMA0484.1chr9:134582132-134582147TGGACTTTGGACCGC-6.19
JUN(var.2)MA0489.1chr9:134583443-134583457AAAGAATGACTCAC+6.1
NFE2L1MA0089.2chr9:134583260-134583275ACATGACTCAGCACC+6.38
Nfe2l2MA0150.2chr9:134583258-134583273CTACATGACTCAGCA+6.83
Nr2f6(var.2)MA0728.1chr9:134584338-134584353CGAACTCTTGACCTC-6.24
RARAMA0729.1chr9:134584335-134584353ACTCGAACTCTTGACCTC-6.22
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00686chr9:134578827-134586282Adipose_Nuclei
SE_04525chr9:134581763-134583038Brain_Anterior_Caudate
SE_04525chr9:134583196-134584452Brain_Anterior_Caudate
SE_09150chr9:134579551-134586375CD14
SE_10884chr9:134578645-134586673CD20
SE_14804chr9:134582888-134584251CD4_Memory_Primary_7pool
SE_17952chr9:134582822-134589309CD4p_CD25-_CD45ROp_Memory
SE_18769chr9:134582861-134586789CD4p_CD25-_Il17-_PMAstim_Th
SE_19472chr9:134583310-134584259CD4p_CD25-_Il17p_PMAstim_Th17
SE_20363chr9:134583141-134584353CD56
SE_22914chr9:134582931-134584438CD8_primiary
SE_27117chr9:134583170-134584009Esophagus
SE_30786chr9:134583043-134584279Fetal_Muscle
SE_31710chr9:134578874-134582349Gastric
SE_31710chr9:134583451-134584107Gastric
SE_32578chr9:134579764-134584637GM12878
SE_33628chr9:134577230-134584040H2171
SE_36750chr9:134582064-134584444HMEC
SE_36915chr9:134578813-134586435HSMMtube
SE_38234chr9:134581951-134586634HUVEC
SE_40722chr9:134578196-134586143Left_Ventricle
SE_42566chr9:134578769-134584551Lung
SE_49262chr9:134583381-134584566Right_Atrium
SE_50405chr9:134578868-134582484Sigmoid_Colon
SE_50405chr9:134583359-134584213Sigmoid_Colon
SE_52037chr9:134581971-134584280Skeletal_Muscle_Myoblast
SE_52732chr9:134583012-134584184Small_Intestine
SE_54202chr9:134583118-134584240Spleen
SE_58352chr9:134520171-134620333Ly1
SE_58881chr9:134579557-134620273Ly3
SE_60991chr9:134494570-134620113HBL1
SE_62218chr9:134495530-134621458Tonsil
SE_63796chr9:134581971-134584262HSMM
SE_64992chr9:134582081-134584259NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9134583114134584077
chr9134583176134583545
Enhancer Sequence
CAGGACACCA TGCGCTATGA AAAACGGCTT TTCCTTCTGA GATGGACTTT GGACCGCAGT 60
CCCCGGGTCT ATCAGCCCAA ACAAATAAAA CCCTATGCGC CAAAGATGTG CTCCTGGTCA 120
GTGGGGCCTG TGAAGGCTTA AAAACCAGAA CTGCTCTGTT CTCTTCTTTA ATCTCCAATT 180
CACTGTGGAT CTTGAAATCC CTACTACCAA CAGTGGTCCT ACCACTCTTC TCATTTAAAT 240
TACTGAACAC AACTAAACAA AACCACAAAA TAAAACATCA AACCTGTCTG TCTGTATACC 300
CAGCTGCTTC CAATGAAAAT CTTCAGACAT TTTAACTCAT GGTTTTCTAA GGAGAACCAG 360
AGACAATCCA AACGTAAGTA AACATATTAA ATTTCTATTC TAAAAGTGGT GCTTTTAAGT 420
AGTTGGATCA ATGCTGATTT TCTCCTGGCT GGCTGGAGAC ACCAGCCCAC ACGGTGCTGA 480
ATTCAGAAGA GTACCGCATC TTGGTCTGCT TCAGTAAATA CCGGTGTCTG CTAAGGCCCA 540
TTCTGAAGAC ACTGTACTAT GTATGACACA GTCAGAACTG GTTCTTTATT TTAATGTGTA 600
AAAATACATG AAAGAAAGTA TAACAAACCT CATATATCGA TGACCTGGAC TCTAACACTT 660
GTTAAACTTA TCCCATTTTG CTTATCTTAG GTCCCCATTT ATTTATACAG TATATTTTGC 720
TGAACCTGTT TTTTTATTTT GATTTTTTCT TTTTTGAAAC AGAGGCTCTC TCTGTTGCCC 780
AGGCTGGAGT GCAGTGGCAT GACCTCAGCT CACTACAACC TCCGCCTCCT GGGCTCAAGC 840
AGTTCTTGTG CCTCAGCCTC CCGAGTAGCT GGGATTACAG ATGTGCACCA GCACGCCTGG 900
CTAATTTTTG TATTTTTAGT AGAGATGGGG TTTTATCATG TTGGCCAGGC TGGTCTTGAA 960
CTCCTGGCCT CATGTGATCT GCCTGCCTCG GCCTTCCAAA GTGCTGGGAT TACAGTATTG 1020
TTTTTAATTG GAGAAAAGGC ATACAAATTT ATTAACGTGT ATACAGGGAA AATCACAGAG 1080
TGATTATGAT TTTAGAGAGT AAATTATAGA TAGCATAACT CTTCACCCTT AAATACTTCA 1140
GCATGACTAT TCAAAAAAGC ACACACTCCT ACATGACTCA GCACCGTTTC ACACATAATC 1200
ACATGAGCAA CAGTTCCTCA TTATAATCCA CCATGGAGTT CATATTCAAA TTTCCCGAAC 1260
TGTCCCCCAA TGTCTTTAAT AGCCGTTTTG TTCAAACTTG GATCCAATCA AGGATTGCTA 1320
AGGAGTACCC TTTCCAAAGT AACATGTTAG ACAAAAGAAT GACTCACAGA AAGTCAGAAG 1380
GGCTGGAACC TGACAGTAAA TTAGCATCCC ACCTACTTTC TTTTTAAGAG AAAATGATCT 1440
ATGATTTGAC AAACAGCAAC TGCTCTTAAT ATTTCCATGC ATTTTCTTCC AGTTATTTGT 1500
TTTCTTTTCA TAAACACACC CATATATGCA GTTGTGAAAA AACTGTCTTG CTACTGATCA 1560
AATGCTACCG CAACTTCTTC TGGCAAGAGG AGGCAAAGAC CTGGTGAAGT CTCGCATATG 1620
TCATCTCTGG CATGCCTGCC AGCCGGCCGG TCTCCTGGGT CAATAACTGT GATAAAAGGC 1680
CGCTGAGTGC GTCAACAGAC TGTCCTGCAC TGAGACACTA TTAAAGGTCC TTGAGCTCCA 1740
AATGTACCAC TGCACTGCTC TGTGGCCCTG CCAACTTCCT CCTCCTCAAG CTGACATGAC 1800
CCCAAGCCCT AGAGAGACAG AGTAGGTGTT AAGAGAGGCT GTTGTCCCAC TTCCTGGGTG 1860
TCCAGGATGG ATAAATGAAA GATTTTACAG AAAGTACCTT GAAAGTACTT TGGAACTTTT 1920
GGAAGTGCTA TATATTTAAA AGCTGTTAAT AACATTATCT AAATCAAAAA ATATCACAAA 1980
AGCCTCAAAC TCCTAGATAT CAAAGCTTTG ACCTGGGATA TTTCTTTTTC TTTCTTTCTT 2040
TTTTTTTTGA GACAGTTTCA CTCTGTCACC CAGGCTGGAG TGCAGTGGCG CAATCTCGGC 2100
TACTGTAACC TCCACATTCT GGGTTTAAGC GATTCTCCTG TCTCAGCCTT ATGCCTGTAG 2160
CTGGAAATAC AGGTGCCCAC CACCAGGCCT GGCTAATTTT TGTATTATTA GTAGAGACGG 2220
GGTTTCGCCA GGTTGGCCAG GCTGGACTCG AACTCTTGAC CTCAAGTGAT CCGCCTACCT 2280
TGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCCCTG 2320