EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-15841 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr3:46984050-46987060 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs189587938chr346984503hg19
rs78580841chr346986452hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr3:46986495-46986510CCAGGCCAAAGGCCA+6.03
KLF4MA0039.3chr3:46984413-46984424GCAGGGTGTGG-6.62
NKX2-3MA0672.1chr3:46985552-46985562ACCACTTGAA+6.02
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00943chr3:46983643-46987096Adrenal_Gland
SE_11155chr3:46963907-46992913CD20
SE_14564chr3:46984749-46992585CD4_Memory_Primary_7pool
SE_18708chr3:46986099-46991562CD4p_CD25-_Il17-_PMAstim_Th
SE_20061chr3:46985017-46993140CD56
SE_22640chr3:46985615-46991406CD8_primiary
SE_23114chr3:46983008-46987127Colon_Crypt_1
SE_23749chr3:46983035-46987037Colon_Crypt_2
SE_26114chr3:46983078-46991394Duodenum_Smooth_Muscle
SE_27142chr3:46983018-46992857Esophagus
SE_28145chr3:46982939-46992085Fetal_Intestine
SE_28630chr3:46982992-46992260Fetal_Intestine_Large
SE_30558chr3:46984380-46986112Fetal_Muscle
SE_31407chr3:46975429-46987226Gastric
SE_38780chr3:46984005-46987196HUVEC
SE_40617chr3:46975387-46993135Left_Ventricle
SE_42118chr3:46970032-46992962Lung
SE_47478chr3:46983535-46987108Pancreas
SE_48306chr3:46984091-46987099Psoas_Muscle
SE_48684chr3:46982967-46987123Right_Atrium
SE_49453chr3:46983064-46985439Right_Ventricle
SE_49453chr3:46985440-46987089Right_Ventricle
SE_50160chr3:46983018-46987192Sigmoid_Colon
SE_52388chr3:46983042-46987272Small_Intestine
SE_58746chr3:46966845-47032612Ly1
SE_59412chr3:46966960-46998383Ly3
SE_59747chr3:46966600-47033537Ly4
SE_60850chr3:46965041-47030117DHL6
SE_62445chr3:46966331-47033109Tonsil
SE_64772chr3:46984018-46985866NHEK
SE_65471chr3:46977753-46993036Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr34698426746984496
chr34698453946986309
chr34698466646986597
Number: 1             
IDChromosomeStartEnd
GH03I046941chr34698304846992889
Enhancer Sequence
TTTATGTGGA GACTGCAGGC ATCAACCAGA CCCTGCCATT CCTTGGCCAC ACAACCTCCG 60
GGGAGCAGAC TACCAAAACC AGGTCGGAGG CCTGGCCCAG AGAAAGGCTT CTGTCATGAG 120
AACAGATCAA CATGCCCCCC ACCCCAACTC AGGGCAGCTC ATCTCATGGC AACGAGGCAG 180
CGAGAACAAA ATAACTGACC AAGTGACAGC AGCTACACGA GAGAGGTCAA CATGGAACGT 240
GGTTCTTGGG CGATGGGTGA GAGGTTTCCT ACTGAGAGAT GGGCTGGGCA GAATTGGGTG 300
ATACAGCATA GGGGGAGAGA AGTGGGAAGG GCATTCCCGG TGGGAAGCAG AGCTTGAACA 360
AAGGCAGGGT GTGGTCTGAA GAGCATGCAG GTGACTGGGG TTGGGGGAGG GGGTGACAAT 420
GATTGCCAGG TAAGACAGTC AAGGCAGGCA ATGGCCGAAC ACAGAGGGCT CTGGCCGGTG 480
TTCTTAAGCA ATGGAGAAAC CGAGGAGAGA CTGGAGAGAG TTCACTGACC TCTGCTGGGG 540
AAGGCAGGCC CTGGGGTGGA CAGGCAGATG CTTGGTGATG GCCAAAGAGG GAAGGGAGAA 600
CAGAGTATAA ATGCTTCACT GAGAAACAAG TCAGGATTCT CCAAATGGCT CCCAGGGCTG 660
CTGGGACCTG GACGGGGCTT CCACAAGGGC CCTGCTGACA CATGCAGCCC TCCCTGACTA 720
AAGACTAGCC GATGAAGCAA GCCAGAGCCT GCAAATTCTA GCAAAAAATT CCTTCCCAAC 780
TCCCAACCAG CGGACACCCT GAAGGCTACT CCCTGCAGTG CCTACCTCAG GGGAAGGAGC 840
GGCAGACACC TGCCCTGGGT AAGGGCAGAG AAGGAAAAGC AGAAAGGGCT CTTCTTTCCC 900
CACACTGGGC TAGTGGGGCA AGACCCCCAG CCACAAAGAC GACTCCTTTC CACAGGGGTT 960
CTGTTAACCC GAACCACCTG GCAGAAGTAG GTGGGGACTA CGGGAAAGTG TCCAGCCTTT 1020
GGGAGGAGTG CTTTGCAAAT ACCATGCCCT TTCTCGGCTC TCAAGCAAGG TCAAACAGCT 1080
GTCACCACCC TCCTGGAGCC CCAGAGACAT TCAAGTGCCT CAGCAAAGGC CAAGTTATTC 1140
ATTAATAAAT GAGAAAACAC CCAACTATCT AAATGACTTT TAAAAATGCC CAGCAATCTG 1200
GTGGGTGGGG GGCAGCACTA GCTCTGCAGA CAGCATGAGG TTAAAAATGA CCCCAGCCTG 1260
GGATGCTGTG CAAAGAGCAG GGGCTCAAAA AAGATAAAGA TCCACATCTG TGGCAGGAGC 1320
AGGTGAACAA ATGAACAGGC CACACAAGTG GGGGAGATAA GGTGTACCTC AGCCTTCCTG 1380
ACAAAGAGTG ATTCATAAAT AGGACAATGG GCATTCACGG GAAGGAAAAT CGCTTTTGGT 1440
GACACTGGCC TGAATCACAA GATAAGGCCC TTTGCTGCCC GGGATAGTGG AGGGAAGCGC 1500
AGACCACTTG AAGCTCACCC CTACCTGAGA GACTCAAAGA GCCTCAGACC TGGAGGGCTC 1560
GCAGGATCAC CCATTCTAGG TCCTCAGTTT AAGCCATGGG AAAACCTGGG AAATGGCAGT 1620
CAGGGAAAAG GAAAAGATTT GTCCAAAGTC ACAGAACCCA TCAGCGGTAG CTGCAAGTCT 1680
GGATCCAGGT CGTCCTGATG CCTGGCCCTC AGTCTTGCCA AGGAGACGAG AGAGAGGCTA 1740
TCAAGAGTGG AAGAGTGGCG CTGAGTTTCT AAAGAGCTCT GATTCTACCC GCCTCTCCTG 1800
CGCTCCCCAC ACAGTTCAGA CCTGGTCCCA TGTGCTCAGA TGCGGCCACA GCCAGCCCAA 1860
GTCCAAGCCT AGGCCCTGCT GGACACTCAG TAGGAAAGCA GGCAAGGCCC TAGGTGCACA 1920
GCCTCCCCAG GAATTTAGAG ACACTTCGCT CACCCTGAGA CCTTTAAATC AGACTCAATG 1980
CCTCACCACC CCCACTCCCC ACTCAATACC CTTCCCAAAT CTTGCCATCT TCTCCCTCCT 2040
TCCCAATCCC TAGTCTCGTC TACCACCTCC TTAGCTCCCC ACCACAACCA AGCCCCCAGC 2100
CATTCCCCTC CACCCCTGCC TGCCAGCCAG CCTTCCCCTC TACTCTGGAG AATACAGCTG 2160
CCTCCTGCAT TTTTCCCTCT CTTTCTCCAA CCTGTCTCCC CTAAGTCTCT CTTCAACTTA 2220
TCAATCCACA TTCCTGGCCT CCTCTTCAAA GATACTGGTC AGACCACACT GCACCTCCGC 2280
TCAAAGCTCT CACTGGGTCT CCACACCCCC AGGACAACAG CCATTCATCT CGACCTCACA 2340
TCTGCTCTGT CCAGAACACT CTTACACCCC ACATTTTGTC TCAAATCCTG AAATATCTAC 2400
TCTGATAACC CCCAAGAAAA CACACCATCT GGCCAGTCCT AAAGGCCAGG CCAAAGGCCA 2460
CCTCCTCAAA GCAGCCTTCT AAGATTCCCA GGCAAAAGAA TCCTCTGGGC CTACCCAGTG 2520
CATATCAGGG TCTGACCGTA GGCCCAGGGC ACAGGCCTGT GGCCATTCCT ATTCACATGT 2580
AGGCTTTACT ACCCCTTCCC TTCAAGAACC TCTCAGCACG GGGCATCTCC TAGAGCACCT 2640
CAAGGCCTAG CCCAGAGCCT GGGCTAGACA ACCTTCAGAA ATGCTACCAA TTTAACTGCT 2700
ACCCTCTCCA CCAACTCCAG AAGAGTAAAC CTCAGGAACG CTGATGGCTG GAGGGCAGGA 2760
GAGTCATGGT CTGGGCTGGG GCCCTCCCCA TAGCCTATCT GCCTATTAAT GGAGGTACTC 2820
CCCCATTTCT CACCCCTGCC CACATCTCCA CACCTAGACC TTGCACCCCT GCCCTCACCT 2880
CCTCCCAGAG CCTTCAGCAG GAAGAAGCCT TTGAGGCAGG ATTTCAGGGG GTCTCAAATA 2940
CAGCCCTGCT CAGGACAGAG TCTGACTGAC CTGTTTCCTA ATGTTTGAAA TCCTTTTTAT 3000
CAGGGACAAA 3010