EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-19786 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr9:134130880-134132480 
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
CCTGCCTCAG CCTCCTGAGT AGTTAGGATT ATAGGCACCC GCCACCATGC CTGGCTAATT 60
TTTGTATTTT TAGTAGAGAC AGGGTTTCAC CATGTCGGTC AGGCTGGTCT TGAACTCCTG 120
ACCTCGTGAT CCACCCACCT TGGCCTCCCA AAGTTCTGGG ATTACAGGCG TGAGCCACCG 180
CACCCCGCCA GGCCATCAGC TTTTTTGTTT CCTGATGAAA CTGTCTTCTT TTGGGCTCCA 240
AGAGGGGCTT TCCTGTTTGG CCTCATGGCC CAGACTACAG CAAGTCTCTG TCCCATTTAA 300
AACAGCCCCA GAGCAGAAGA GGCTCTCCTG AGAAGTGACT TTGAAAGTGG GAGGTGGAGA 360
TGTTATGGGG TCGCTGTGCA GCTGCTTCTC CCAGACCCTG GATGTCTCAG GCAGGTGAGC 420
CTGGCCTGGC CCAGACAGCC GGCTCTCCCA GGCCCAGATC CTGGAGAGGA ACCCGTGACA 480
GCTGGGCAGA ATCTACTGTC TGTGCCTCTT CTCCCAGTCT GGACTTCTAA ATTTCACCTG 540
CTGTCAGCTG GAGAGGCTGG AGGGCTTCCA CTCTGTGACT AAATGCCACT TGGAATCCAC 600
TTTACTCACA ACTCCCTCCT TGTACATTTC CCTCTCGAAA CTGTTACCCA CAGATTCAGC 660
TGCGTCTCCC CATCTCCCGT CTCACTGCGC CTCTGCATGA AGGCTTTGCT CTCCTGAGCT 720
TCTGAAACCC TGCTATCAGG TTAGGCCTGC ATCCCATTCT CTGTACACAC ACACACACAC 780
ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACACACACCA TAGTCTCTCA 840
TGGGCAGAGC TCAGGAGCCG ACTCCACACC GAGAAGCCAA ACCACGACAG TGAACTGCAC 900
CACCCAGGAG CCATCTGCGT GGAGCTCGGC CAGCAATGCC TGTTATGCAA TTTCCTGCTT 960
TGGTGTCTCA GCCCCAGGAG GCAGGATGTG AGCGCCGTTG GTTTGCTGCA ACGTGGAGAA 1020
CCCACAGAAG ACCCGAATTC TGATGCCCAG AGTGCATGGG GCCTCCCTGT CCCCGTGGGG 1080
GTGCAGAGAA GCCACTGCCC ACCCTGGATG ATGAGCCTGT GTGCGGTGGG TGCAGCAGCC 1140
GGCCCCTGCT CAAAGGGAAT CAGATGGGCT CATTGTGGGC CAGAAAGAAC TGACTGCCCC 1200
GAGACTTCCG GGGTGGGGAG GGGGGTGCAC TTCCTGCCCG GGGCACCCAG GATGGGGGAG 1260
CAGAGGCCTG GGACCTTCTC AGTAACAGTC ACCAATGTTA TTGGACACTG CACATGGCCC 1320
CACCGTCTCA GGCTCAAGAC TGAGAGTGCG CTATGGCGAG AGGTGGCTCT GTGGCCAGAG 1380
TTCGAATCCT GGCTCCGCCT TCCCCTAGCT ATGTGGTCTC AGGCAGCTCC TTGGCGTCCA 1440
CTCTCCCCGT TCCTTCGTCT GTGAAATGGG GGTGGCAGTT AACACCTCCC TTGTGGGGTT 1500
GTCATGAGGA TTCAATGAGT TCGCACCCAG AAAGAACAGG GAGTTTCCAC TGAATCCGCC 1560
AGGAGGCAGC TCCTCTGAAA ATCTCCATTT TCTTTTTCCT 1600