EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-83726 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr9:134130830-134132470 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr9:134130990-134131005TGAACTCCTGACCTC-6.22
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_09361chr9:134126808-134138940CD14
SE_10759chr9:134130225-134133328CD19_Primary
SE_11405chr9:134127138-134155283CD20
SE_12146chr9:134130208-134133493CD3
SE_13249chr9:134131782-134132497CD34_Primary_RO01480
SE_13579chr9:134131058-134133449CD34_Primary_RO01536
SE_14464chr9:134130006-134133411CD4_Memory_Primary_7pool
SE_15482chr9:134130757-134132926CD4_Memory_Primary_8pool
SE_15960chr9:134130241-134133433CD4_Naive_Primary_7pool
SE_16450chr9:134130517-134133034CD4_Naive_Primary_8pool
SE_17086chr9:134130919-134132783CD4p_CD225int_CD127p_Tmem
SE_17445chr9:134129893-134155392CD4p_CD25-_CD45RAp_Naive
SE_17921chr9:134128949-134133914CD4p_CD25-_CD45ROp_Memory
SE_18747chr9:134130406-134134742CD4p_CD25-_Il17-_PMAstim_Th
SE_19407chr9:134130269-134134369CD4p_CD25-_Il17p_PMAstim_Th17
SE_20268chr9:134127140-134134040CD56
SE_20819chr9:134130581-134133004CD8_Memory_7pool
SE_21594chr9:134130488-134133494CD8_Naive_7pool
SE_22019chr9:134130594-134133078CD8_Naive_8pool
SE_22737chr9:134130058-134134193CD8_primiary
SE_25701chr9:134127131-134134558DND41
SE_29891chr9:134130804-134132623Fetal_Muscle
SE_31045chr9:134130157-134132601Fetal_Thymus
SE_40648chr9:134130930-134132557Left_Ventricle
SE_42331chr9:134128984-134132556Lung
SE_43702chr9:134130117-134133808MM1S
SE_48088chr9:134131013-134133521Psoas_Muscle
SE_48582chr9:134128933-134132591Right_Atrium
SE_49606chr9:134131461-134132254Right_Ventricle
SE_50385chr9:134130947-134132571Sigmoid_Colon
SE_51267chr9:134128852-134132710Skeletal_Muscle
SE_52980chr9:134130955-134132577Small_Intestine
SE_53628chr9:134128994-134133668Spleen
SE_55150chr9:134130991-134132503Thymus
SE_59220chr9:134127420-134154306Ly3
SE_61761chr9:134100900-134154925Toledo
SE_62280chr9:134108336-134154785Tonsil
SE_67312chr9:134130117-134133808MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9134131233134132425
chr9134131602134132161
Number: 1             
IDChromosomeStartEnd
GH09I131251chr9134126988134134384
Enhancer Sequence
GTACAGTCTC GGCTCACTCC AACGTCTGCC TCCTGGGTTC AAGCGATTCT CCTGCCTCAG 60
CCTCCTGAGT AGTTAGGATT ATAGGCACCC GCCACCATGC CTGGCTAATT TTTGTATTTT 120
TAGTAGAGAC AGGGTTTCAC CATGTCGGTC AGGCTGGTCT TGAACTCCTG ACCTCGTGAT 180
CCACCCACCT TGGCCTCCCA AAGTTCTGGG ATTACAGGCG TGAGCCACCG CACCCCGCCA 240
GGCCATCAGC TTTTTTGTTT CCTGATGAAA CTGTCTTCTT TTGGGCTCCA AGAGGGGCTT 300
TCCTGTTTGG CCTCATGGCC CAGACTACAG CAAGTCTCTG TCCCATTTAA AACAGCCCCA 360
GAGCAGAAGA GGCTCTCCTG AGAAGTGACT TTGAAAGTGG GAGGTGGAGA TGTTATGGGG 420
TCGCTGTGCA GCTGCTTCTC CCAGACCCTG GATGTCTCAG GCAGGTGAGC CTGGCCTGGC 480
CCAGACAGCC GGCTCTCCCA GGCCCAGATC CTGGAGAGGA ACCCGTGACA GCTGGGCAGA 540
ATCTACTGTC TGTGCCTCTT CTCCCAGTCT GGACTTCTAA ATTTCACCTG CTGTCAGCTG 600
GAGAGGCTGG AGGGCTTCCA CTCTGTGACT AAATGCCACT TGGAATCCAC TTTACTCACA 660
ACTCCCTCCT TGTACATTTC CCTCTCGAAA CTGTTACCCA CAGATTCAGC TGCGTCTCCC 720
CATCTCCCGT CTCACTGCGC CTCTGCATGA AGGCTTTGCT CTCCTGAGCT TCTGAAACCC 780
TGCTATCAGG TTAGGCCTGC ATCCCATTCT CTGTACACAC ACACACACAC ACACACACAC 840
ACACACACAC ACACACACAC ACACACACAC ACACACACCA TAGTCTCTCA TGGGCAGAGC 900
TCAGGAGCCG ACTCCACACC GAGAAGCCAA ACCACGACAG TGAACTGCAC CACCCAGGAG 960
CCATCTGCGT GGAGCTCGGC CAGCAATGCC TGTTATGCAA TTTCCTGCTT TGGTGTCTCA 1020
GCCCCAGGAG GCAGGATGTG AGCGCCGTTG GTTTGCTGCA ACGTGGAGAA CCCACAGAAG 1080
ACCCGAATTC TGATGCCCAG AGTGCATGGG GCCTCCCTGT CCCCGTGGGG GTGCAGAGAA 1140
GCCACTGCCC ACCCTGGATG ATGAGCCTGT GTGCGGTGGG TGCAGCAGCC GGCCCCTGCT 1200
CAAAGGGAAT CAGATGGGCT CATTGTGGGC CAGAAAGAAC TGACTGCCCC GAGACTTCCG 1260
GGGTGGGGAG GGGGGTGCAC TTCCTGCCCG GGGCACCCAG GATGGGGGAG CAGAGGCCTG 1320
GGACCTTCTC AGTAACAGTC ACCAATGTTA TTGGACACTG CACATGGCCC CACCGTCTCA 1380
GGCTCAAGAC TGAGAGTGCG CTATGGCGAG AGGTGGCTCT GTGGCCAGAG TTCGAATCCT 1440
GGCTCCGCCT TCCCCTAGCT ATGTGGTCTC AGGCAGCTCC TTGGCGTCCA CTCTCCCCGT 1500
TCCTTCGTCT GTGAAATGGG GGTGGCAGTT AACACCTCCC TTGTGGGGTT GTCATGAGGA 1560
TTCAATGAGT TCGCACCCAG AAAGAACAGG GAGTTTCCAC TGAATCCGCC AGGAGGCAGC 1620
TCCTCTGAAA ATCTCCATTT 1640