EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS094-42522 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr9:33139000-33141430 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3780486chr933139453hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr9:33139223-33139240TGCCTTCCAGGAGTTCC+6.02
NFYBMA0502.1chr9:33140242-33140257CTGATTGGCCAGTGG-6
RARA(var.2)MA0730.1chr9:33141277-33141294AGGTCACCTTGAGGTCA+7.71
ZNF263MA0528.1chr9:33139345-33139366CTCTTCTCACTCTCCTGCTCC-6.41
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00330chr9:33138866-33141700Adipose_Nuclei
SE_00992chr9:33138818-33140399Adrenal_Gland
SE_00992chr9:33140510-33141415Adrenal_Gland
SE_10229chr9:33134720-33146706CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_12090chr9:33136393-33139356CD3
SE_12090chr9:33140249-33142158CD3
SE_14891chr9:33140511-33142287CD4_Memory_Primary_7pool
SE_18081chr9:33140148-33141844CD4p_CD25-_CD45ROp_Memory
SE_18665chr9:33135758-33139718CD4p_CD25-_Il17-_PMAstim_Th
SE_18665chr9:33140056-33142210CD4p_CD25-_Il17-_PMAstim_Th
SE_19329chr9:33140372-33141391CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33134255-33146063CD56
SE_22416chr9:33135220-33146719CD8_primiary
SE_26031chr9:33139672-33141321Duodenum_Smooth_Muscle
SE_26859chr9:33139260-33140484Esophagus
SE_26859chr9:33140490-33141363Esophagus
SE_27770chr9:33139911-33141110Fetal_Intestine
SE_29800chr9:33139312-33141840Fetal_Muscle
SE_31534chr9:33139337-33140430Gastric
SE_31534chr9:33140552-33141138Gastric
SE_32659chr9:33135226-33145795GM12878
SE_40894chr9:33138811-33142004Left_Ventricle
SE_41831chr9:33139282-33140314LNCaP
SE_42236chr9:33137933-33140413Lung
SE_42236chr9:33140421-33142021Lung
SE_44340chr9:33139198-33141245NHDF-Ad
SE_45447chr9:33139306-33141157NHLF
SE_45731chr9:33138938-33141879Osteoblasts
SE_46917chr9:33138775-33140378Ovary
SE_46917chr9:33140576-33141301Ovary
SE_47814chr9:33139478-33140178Pancreas
SE_48426chr9:33138706-33140393Psoas_Muscle
SE_48426chr9:33140480-33141409Psoas_Muscle
SE_48738chr9:33136686-33140472Right_Atrium
SE_48738chr9:33140483-33141323Right_Atrium
SE_50176chr9:33134918-33140478Sigmoid_Colon
SE_50176chr9:33140489-33142097Sigmoid_Colon
SE_51651chr9:33138989-33141643Skeletal_Muscle
SE_52621chr9:33139293-33140398Small_Intestine
SE_52621chr9:33140511-33141315Small_Intestine
SE_53402chr9:33139080-33142103Spleen
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr93313932133140496
chr93314069633141208
Number: 1             
IDChromosomeStartEnd
GH09I033133chr93313369733146567
Enhancer Sequence
CATGCCGGGG CTGTCCACAG CATGCTGACA ACCCACAGAA GCCGATCGAG CACCAAGCCA 60
GAGAGTCTTT ACTCTGAAAT GTCTGTTAAC TGCAAACTTG CCCTGTGATA TGTATCAAGA 120
CCACTTTCAA TTTGTTTCAA TTGATACTTT CTGGGTACCT ACTGTGTGCC AGCCCAAGGA 180
GGAGTGGGTT GAGGTAGGGA GGGAGGATGG ACAAGACAAA TCCTGCCTTC CAGGAGTTCC 240
CTGCTGAGCG TGTGGCAGAA CCTAAATGAA AATTACCCTG GTTTAAGGAT GGTCAAGGAG 300
CTTGCTCCTC CAATGGCTCT GTGCAGAGCT TTATCACTGA ACAGCCTCTT CTCACTCTCC 360
TGCTCCCTTC TGAACTCGCT GTGCCCCTTG CACAACCCCC ATCATGCTTC CAACACACTG 420
AGACACCTTG ACCCCCAATC CTGCCCTTCT TGCCAATCTG GCAATTTTTT CTCCACAACT 480
CTAAGGATCT TGCAGCTCAC ACCTTTGAGA CAACAGACAG CAGCCCCAGA CCTGGCGTTG 540
AATGACTAAT TGGGTCGAGT GCCAGCCAGG AGGCCTCCTG AATGCCCTGC ACACCTCCTG 600
CCATACTGCA GGGACCATGC TCTGCTACAC ACCTGGCTCT GTCCCAGTGA GAAACTCCAG 660
AGAGCTCAGA CTCCAGGAAG GCAACGACTA CCTCTGTTCA GAATCATGCA GACCTGCGAC 720
CAGGTTTCAG AGCCACTGCC TGGGGTGGTG GGGAGAAGCT CTGGGAGGAG GCAGAGGGCT 780
GAGGGCTTCA TGACAGGCCT CAAGCCGAGC CAAGGCGCCC TTGCTGTGCG GCGCATGGCG 840
TGTGCTACCA CAGGCTCTCG GCCCCGCTGG GCTGGCTTGT GTGTTTTCTT GGCTCTGGAA 900
GCTGGGAGGC AGGGTTACGT AAGCAGATGA GCAGATGTAA GCTGTCCTCG GCTCCCCCAG 960
CTCAAGCCCC GCCACGTGGG CCTCTCGGCT GGGAGTCCAG GTCATGGCCT TGCATGTAAG 1020
TCGCTCAATA ACTTCAATGT GTGAGCTCAA TTCAGACAAA TTCCACTGCT CCCCTGCCTG 1080
GCACAGCAAA CCCAAACACA TACATGCCCC TCCATCAAAG GCCCTGCTAA TCTAAGCCAA 1140
CACCAGCACG GACTCCTGAC TGGTTTTCAT GCTGGCTGAA GCACTAGTTC AATCCTTTAG 1200
CCTCAGCAAA ATAGGCTGAA ACATCTAGTC ACTGTTTGTC AACTGATTGG CCAGTGGGTC 1260
GAAAGAAGCG TTGGCCTGAT GCTTTATTGT GACAATGTTT CACTAGCCCA GGAATGAAAT 1320
CACAGAAGTA AAGACCATGT AGGTGTTTTT TAATTAAACT AAAGGTAATC AAAGTATAGG 1380
AATGCCCTTT CTTCCAAGAT TAAGTGCTTC TTACTCTTTG AATATTAAAA TGTCCTTTCT 1440
CTTATGAAAT CATCATAGAT TTTCATGCTG GACTGATTTT TAAAATTTAA TTTAAAAAAA 1500
AAATCCTTCC TTGGCAGCCA TGGGTCAGGC CTCTAAGTTT GTTTTGAAAA TTCTCTGGAC 1560
AGGAAATCCA AGTATTCAGG AAACATTTGG GAACACGTGG AACTAGGCAG TGCCTAGAAC 1620
TCTGTGATTC TGAGAGCTGG GATACTGGAA TTTCTTCCTG GGTCTCAGAC CTGACAGTAC 1680
ACTGCACAGC CCCTCTTCAC AAATCAGCTC CCCCACCAGT GCTGTTCCAC AGGCTCATGT 1740
GGATGGGCCG CTTCTCTCTG TACCAATCTT CCAAAGGCCA GGTGCGCACC GCAAGCTGAG 1800
CCAGGCATTA CCACCAAATT CCCCAGCTTG AGAAAAGATT TGCTTGCAGC ATTCTCGTGA 1860
AATCACGGTG CCCCTTGAGG CCCCTTGGGC TAGAAATGAG AAGCACCATT TACTGTACGT 1920
GGCTCACCCG TCATTCTGGG AAGAGCACAA GCTCTCTAAG TCTGCAAGGG CTTCAGTCTA 1980
ACAAATCTAA CAGCTGCCTG GCCTTAGCTC AAACACCACC CTCCCAGGAA GCCTTCCCAG 2040
ACCACTCAAG GTTGGTTCTT AAGCATTTCA CCCACTTCCC CTAAGCATTC ACAGCACCAC 2100
ATCCATTCAT ATTCAAACAT GTACCCAGTT AGTATGTATC ATGTGCCAGG TGGTATAGGG 2160
CATGCAGGGG TTGGTAGGGG AGTGGGCGGC AGGGTGAGCA AGTAAAGAAG AGGTCTTTGA 2220
GGCTGGGCAT GGTGGCTCAT GTCTGTAATC CCAGCACTTT GGGAGGCTGA GACAGGCAGG 2280
TCACCTTGAG GTCAGGGGCT TGAGACCAGC CTGGCCAACA TGGTGAAACC CCATCTCTAC 2340
TAAACCCCAT CTCTATTAAA AATACAAAAA TTAACCGGGT GTGGTGTAGC TGTAATCCCA 2400
GCTACTTAGG AGGCTGAGGC AGGAGAATCT 2430