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

TagContent
EnhancerAtlas ID
HS044-08878 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr3:46973030-46974250 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SOX10MA0442.2chr3:46973700-46973711AAAACAAAGCA+6.02
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00943chr3:46971562-46975179Adrenal_Gland
SE_02008chr3:46971380-46975339Aorta
SE_10127chr3:46964000-46982704CD14
SE_11155chr3:46963907-46992913CD20
SE_13638chr3:46971550-46974655CD34_Primary_RO01536
SE_14564chr3:46971566-46975300CD4_Memory_Primary_7pool
SE_18708chr3:46972575-46975234CD4p_CD25-_Il17-_PMAstim_Th
SE_20061chr3:46970016-46975395CD56
SE_22640chr3:46971928-46975052CD8_primiary
SE_23114chr3:46971617-46975208Colon_Crypt_1
SE_23749chr3:46971711-46973448Colon_Crypt_2
SE_23749chr3:46973449-46975042Colon_Crypt_2
SE_26114chr3:46971685-46975312Duodenum_Smooth_Muscle
SE_27403chr3:46970664-46979932Esophagus
SE_28630chr3:46971492-46975383Fetal_Intestine_Large
SE_30558chr3:46971654-46978550Fetal_Muscle
SE_31407chr3:46970646-46975250Gastric
SE_32585chr3:46966448-46975230GM12878
SE_38780chr3:46970749-46974865HUVEC
SE_40617chr3:46970726-46975377Left_Ventricle
SE_41619chr3:46971597-46975216LNCaP
SE_42118chr3:46970032-46992962Lung
SE_47478chr3:46971661-46973453Pancreas
SE_47478chr3:46973781-46974777Pancreas
SE_48306chr3:46971528-46975218Psoas_Muscle
SE_48684chr3:46971559-46975364Right_Atrium
SE_49453chr3:46972817-46973621Right_Ventricle
SE_49453chr3:46973793-46975177Right_Ventricle
SE_50160chr3:46971539-46975248Sigmoid_Colon
SE_52388chr3:46971545-46975260Small_Intestine
SE_53507chr3:46970696-46975269Spleen
SE_58746chr3:46966845-47032612Ly1
SE_59412chr3:46966960-46998383Ly3
SE_59747chr3:46966600-47033537Ly4
SE_60850chr3:46965041-47030117DHL6
SE_62445chr3:46966331-47033109Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr34697321646973514
Number: 1             
IDChromosomeStartEnd
GH03I046924chr34696632946982223
Enhancer Sequence
GGGCGCTAGC CTCCCTTCTC ATCCCTTATA TCTTGAGGCT ACTCCACATT CACCTGCTGC 60
CCTGGGCCCC TGGAGGGAGG CAGAGAGGAT AAGGACAGGA CAGTCCCACA TGGCCTGTTC 120
CCTGAGAACA AGGTCCTCCA CCTGGCCACC CTGGTCCCTC CTGGCCATAC AGGCCCCATC 180
AAGGGCCAGA GAGAGAACTG CTGTGAGGCA CTCCTCCTAG TAACAGACCA CAGGGAAGGC 240
CACGCCCAGG ATGCGCCTGC AGGCCTTGCA GAGGCCACCA CTGACCAGAG AGACTGGCAA 300
CTTTGATCAA AGAACACTTT CATTTTTAAT ATTCAGAGTA CAGAGACACT GGAGCTCTGC 360
CAGGAAAACA CACTCATGAC ACTCAGACAT GCCCCTAATA ATCCTCTGTT TGCTTTAGGC 420
TCTGCACATA GAGACCTACC CCTTGTCCCC AATATAAATA ACAAGGCTTC AGTTGCTGCT 480
GCCAGAGGCC AGACTCGACA GAAGCATGAA AATGAGGGGA GAGGCAACTA CCCCAAATGA 540
GGTACACAAC TGCTCTAGAG GCTGATCTGG TCTTTCTTTC AAGGGCCATT AAAATGTTCA 600
AACTCCCTGA CCCGGTAACC CTGCTCTGGG GAAATTATTC CATAGAAATA GTAACAAGAC 660
AGGAGCAAGC AAAACAAAGC ATTCTATATA CGCACGATCC TGGCAGCATA ATTCATAATA 720
GCTACAACAC CTCTGGGATC TCTTCTGGCA GAGTGCCCTA GAGTGGCCTA AAGTACCACC 780
AGGCTATGAG GGCAAAGGAC AATTTAGTAC AGGGATGTTT TTGTTTGGTG GTTGATATTT 840
TTCTTTAGAA CACTCAATGG CTGGCTTTGC AGCAAATGAG ACTTTTAAAG AGCCCAGTGG 900
CTTCCCCACT CGTGGGCAGA GGAGACTGTC CTCCAGCTGT CACCCAGCAA GGCAACTGTG 960
GCCCCAGCCT GAAGAACGGG TACAGTGTAA GGCAATAAAA CCTCCCTTCC CTTCTCTTAT 1020
CCAGCCCACC CCAAGCCTCC TGTCCTTCTG GCCACACAAA GAGGACAAGG TCTATTGGAG 1080
CACATGACAC AAGAAGTGAC CATGGGCAGG ACAGGGCCAC ATCACAGCCT CAGGGGGTGG 1140
ACAGGCCTCC AAGCAAGTCC TGGCAAATGC GTCCTCAGCG GGTTTCAGAA AAAGGAGTGG 1200
GAGCGCCTTT GTGCCCCCAC 1220