EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS056-02384 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr11:35186560-35188680 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NKX2-3MA0672.1chr11:35186717-35186727ACCACTTGAA+6.02
Spz1MA0111.1chr11:35188091-35188102AGGGTAACAGC+6.62
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00768chr11:35183057-35193176Adipose_Nuclei
SE_01864chr11:35187561-35188918Aorta
SE_09182chr11:35178707-35190909CD14
SE_10283chr11:35181082-35190379CD19_Primary
SE_10949chr11:35158702-35203324CD20
SE_11836chr11:35179165-35193252CD3
SE_14392chr11:35179788-35193448CD4_Memory_Primary_7pool
SE_15437chr11:35184640-35190696CD4_Memory_Primary_8pool
SE_15845chr11:35184951-35190138CD4_Naive_Primary_7pool
SE_16300chr11:35183501-35190823CD4_Naive_Primary_8pool
SE_16879chr11:35180422-35190989CD4p_CD225int_CD127p_Tmem
SE_17331chr11:35158731-35197607CD4p_CD25-_CD45RAp_Naive
SE_17796chr11:35158420-35197707CD4p_CD25-_CD45ROp_Memory
SE_18259chr11:35158690-35193712CD4p_CD25-_Il17-_PMAstim_Th
SE_19135chr11:35177404-35192755CD4p_CD25-_Il17p_PMAstim_Th17
SE_20092chr11:35180463-35193382CD56
SE_20772chr11:35180763-35190826CD8_Memory_7pool
SE_21480chr11:35183642-35193202CD8_Naive_7pool
SE_21936chr11:35179831-35192692CD8_Naive_8pool
SE_22358chr11:35169620-35193482CD8_primiary
SE_25914chr11:35186276-35193173Duodenum_Smooth_Muscle
SE_26946chr11:35186352-35190653Esophagus
SE_30464chr11:35186866-35190821Fetal_Muscle
SE_34152chr11:35186061-35189843HCC1954
SE_35960chr11:35183206-35190542HMEC
SE_38888chr11:35184738-35190385IMR90
SE_43291chr11:35187615-35189892Lung
SE_44009chr11:35183586-35190352MM1S
SE_44168chr11:35178434-35194119NHDF-Ad
SE_44840chr11:35184516-35190436NHLF
SE_45750chr11:35181937-35193958Osteoblasts
SE_47126chr11:35156596-35197662Panc1
SE_50277chr11:35183542-35192586Sigmoid_Colon
SE_52892chr11:35186228-35190724Small_Intestine
SE_54000chr11:35183547-35190826Spleen
SE_54856chr11:35186815-35193194Stomach_Smooth_Muscle
SE_55234chr11:35184824-35189727Thymus
SE_56393chr11:35182218-35191462u87
SE_58845chr11:35127651-35209995Ly3
SE_61083chr11:35126857-35205408HBL1
SE_62267chr11:35127535-35205945Tonsil
SE_64329chr11:35182714-35190021NHEK
SE_67549chr11:35182218-35191462u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr113518694635187176
Number: 1             
IDChromosomeStartEnd
GH11I035157chr113517905935197546
Enhancer Sequence
GACTTTTCCA CCAAGGCTCT TAGGGCTTTG TGGTGGGTGC CAGAACAATT GATGGGGTAG 60
GGTGGGTGCT GGAAGAGAAT GAGCATCTGG TAGATTGAGT CTCTGGGTCT GCCCTTCCAC 120
CCTCACTCCA GCCCCCATTA GCTCAGCTTG ATTTTCAACC ACTTGAAATA CTGTGGTTGT 180
GCCTAAGACA TCATGTCAGG GAGAGAAAGA AACATCTGAA AACCATCAAT CTTCTCTCTG 240
AATGCTTCCA CTGGTCCCAT TTGCCTGTTG ACAACCCAAG TTGAAAAGGC AGCACCAGAG 300
GGGAATGGGG AAAATTAGCA GAACTGGAAA ATCTGAGTTG AGATCTGGGT TTACCAAACT 360
CTCCGTAAGA CTTTGAGTCT GTGAAACTTA TGTCCATTAG TTTCTTCACC TTTTAAATGG 420
GTCTGTAGTA CCTACCCTCT GGGCCTCACA GGCTGCTTTT GGGTGTGAAA GTGCTTTATA 480
ATTGGTGAAG GAAACTGCTA CGTGGCAAGA ATAGCAAAGC CTGATGTACT TTAATCCATT 540
CGGTTCTGCT GAGGGTGGAG CCCCAATGTG TCTTAATTCA TATGAGGTTT CTGAGAAGCT 600
TTTTGAGATT TTAATACTGT CCCAGGTATG CACATCAACC TTCTCACTTT TATCCCCCAA 660
GCTCCAAAAT TTCATAACTT TTTATTTCAT CTTGGGTGGC AGGAAGGCAA GGTGTGCCTG 720
GGGGAGCTAC AGGGAGTTAT TCAAGGTCAC ATAATTAGCT TATAATTAAC AGAGTTTAGG 780
CTAGAACCAG TGCATCCCAC TCCCAGATGG GGGCCCCCGG CTTATCTCAG CATGTCAGCA 840
ACCCATGAAT CAGCCCTGAA ATATAGATAT TACCTATGAG TAACAGTTTC TCATCCTACC 900
TCAACTGTTA CGAAAGTCTT CCCTCAAACT AAAGCTAAGC AGTTCCACAA AATGCCAGCT 960
ATAGACATTA GCAGAAACTG TATATTGATT AGGTGATGTA TCAGTCATTG TAACTACCCA 1020
GAAAAAAAAA TACAATGACA AAACCAAGTG GCCCAACCTT ATTTTCTACT TGCAAGAGGA 1080
AAAACCCTAT TTGGGCCCCA AGATGCTTTT TTCATTTCAT TTACCACATC CTGGGTTTGT 1140
GCTAGTCAAT CTGCTAAATC AATAAGATCC GAAAAAGCAG AAAACAAAGA TCGTGAGGCC 1200
AGAGGATTTC CTGATCACCA TGGCAACACA CAGGGGTGGG TACTGTGGTT TCTCTGCCTG 1260
AAGACGCACT CGTCAAAGAC TACTTGGTGT TACAGAATTC TGGTGCAGTG AAGCAACAGT 1320
TCTGGGACAT ATACTTTCTT TTGCCAGAAA GACTCTGTTG GATCCAGGAC CAGGAGTGGG 1380
GGGTTAAACA GTTCTCCATA CCCTCACCTC CAAGTCCCCA TCATCCCATT AGGAGACAGG 1440
GACAGTACTG TTCTCCAAAC TCTCAAAACA ACCCAAGAGC TTTCTAGGCT GTGCATTGGG 1500
TTGATCATTT GGTGGCCTTG GCTGAAGGGC CAGGGTAACA GCTAGGAGAA CCCTTGGGAT 1560
TCTTCTCCAA TGTGACAGGC CCCTCCATGT TGGTTCAGCG TTGACTGCCA TGACAGGCTC 1620
CAGGCTCCAC GGAAAAAAGG CAGAGAAATC AGGGGGTCCA GCCAGGCGCC AAGACGTTGG 1680
GGTGCCTTGC ATTTCTAAGT GCCAAGTGAT GAATAGCTCA GTTGAAAGCA ACCCAGGGCA 1740
CATTCTGGAG GAAATTCTCT GGGTATGATT GTGCATGACT GTTTTCTCTG CTCATTAAAC 1800
CCTCATCTGC CTCCAGGGCA ATTCCGGGAG AGACTGAGTC ACTCAAGACT CATGGTCTGC 1860
ACTGGGCAGC CAAAGGCGAT TCGGCCACCA AGTGTGATTC TGGCCTCATT CAGAAGTGGA 1920
TGCTAAACAA TACACCCTTT CACCAGGAGC CCATCACATG GGCATCAGGA GATGGGGGCG 1980
AGTGATGTGC CAGCCTTCTA GACTGGCAGG CCTGGGGGGC AGCAGAGGGC ACAATAGCTA 2040
GAAAGACTCC CAGATGAAAA CTTCTGGGCT TTGAAGCCTT CGAACAAATG AAGAAGAAAA 2100
TGACTTCTTC GTGTCCTATT 2120