EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-15842 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr3:46987840-46991370 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs13092573chr346988561hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr3:46989860-46989871AGAGATAAGGA-6.02
NR2F1MA0017.2chr3:46989541-46989554CAGAGGTCATGGG+6.22
RARA(var.2)MA0730.1chr3:46990879-46990896AGGTCACACAGAGGGCA+6.61
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00943chr3:46987333-46991985Adrenal_Gland
SE_02008chr3:46987772-46990525Aorta
SE_11155chr3:46963907-46992913CD20
SE_13638chr3:46988105-46991652CD34_Primary_RO01536
SE_14564chr3:46984749-46992585CD4_Memory_Primary_7pool
SE_16650chr3:46987830-46991302CD4_Naive_Primary_8pool
SE_18708chr3:46986099-46991562CD4p_CD25-_Il17-_PMAstim_Th
SE_20061chr3:46985017-46993140CD56
SE_22640chr3:46985615-46991406CD8_primiary
SE_23114chr3:46987260-46991352Colon_Crypt_1
SE_23749chr3:46987346-46991294Colon_Crypt_2
SE_26114chr3:46983078-46991394Duodenum_Smooth_Muscle
SE_27142chr3:46983018-46992857Esophagus
SE_28145chr3:46982939-46992085Fetal_Intestine
SE_28630chr3:46982992-46992260Fetal_Intestine_Large
SE_30558chr3:46988988-46991255Fetal_Muscle
SE_31407chr3:46987243-46992180Gastric
SE_32585chr3:46989343-46991413GM12878
SE_38780chr3:46987824-46991550HUVEC
SE_40617chr3:46975387-46993135Left_Ventricle
SE_41619chr3:46988621-46991305LNCaP
SE_42118chr3:46970032-46992962Lung
SE_47478chr3:46987822-46991381Pancreas
SE_48306chr3:46987919-46991489Psoas_Muscle
SE_48684chr3:46987782-46991986Right_Atrium
SE_49453chr3:46987803-46989682Right_Ventricle
SE_49453chr3:46989698-46991296Right_Ventricle
SE_50160chr3:46987309-46992159Sigmoid_Colon
SE_52388chr3:46987277-46992190Small_Intestine
SE_53507chr3:46987802-46992203Spleen
SE_58746chr3:46966845-47032612Ly1
SE_59412chr3:46966960-46998383Ly3
SE_59747chr3:46966600-47033537Ly4
SE_60850chr3:46965041-47030117DHL6
SE_62445chr3:46966331-47033109Tonsil
SE_64772chr3:46987179-46991025NHEK
SE_65471chr3:46977753-46993036Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 7             
ChromosomeStartEnd
chr34698953346989702
chr34698793146988653
chr34699043746991167
chr34698877546989017
chr34698868646990431
chr34698973646990203
chr34698840746991335
Number: 1             
IDChromosomeStartEnd
GH03I046941chr34698304846992889
Enhancer Sequence
ACACTTAGGG AATTAGCAAG GGATAGGTGT TGTCGGGGAA GGAAGTAATG CTTAAACTCA 60
ATTCTAAATG TCCACTGGGG GATTATGAGG CAGCTAAAGA AGGCAGAGCA TTCCTGGGAG 120
TGGTAACTGC CTACAAAGAC ATGAGAGCGG AGCAAGAGCA CTGTCACAGC CTGCAGAGCA 180
GGCCCACATG GCTGGCCCAG CCTCACCTGA TGCTGTCAGG GGCAGGGCTC ACAGGGCATT 240
CCTCCAGCAC CGTGGGAGGG CTGAGCCCAG CATGAGGGCC GACACCCTGA ACGGGCACTG 300
TGGTAGCCTA CAAGATGTGT CATGGGAGGA ACGGGGAAGA CCAGAAGTCA GGTGAGATCC 360
TCCACTCCCA GCCTGGACCT GCCCCAGCCT GCTGCTGTCT GTGTGTCTGT GTTTGGGAGG 420
GGGGTTAAAG TTAAAATGAG GGCTGGGAAC TGTCACTGGG GGCGGGTGTG CCGAAGCAGG 480
AGGACTTGAG TTCAGGGGAT GAGGAATAAG CCCCTCCCTC TCCCTAAGAC TTCCCAAGGA 540
CTCAAACTTT TAGGAGCTGC TGACTAGAGC TCTCCCTTCC AGAAGGAAAT AAGAGAAGCA 600
GGAAAGGGTT AAGAGAGAGA CATTCAACTT CTCATCTAGG GTCTTCCCAC CCTTCTTTAG 660
CTTCCTGAAG AAGCTAGAGA CTCACCAGGA ACTCATGGGT ACAGAAACAC TTTCCAATCC 720
CCAGGTGATA TGCCCCATTA GCTCTGAGTA CGCCTGCTAT AATGTCCATG GGAAACTGCC 780
CTCTGTTCAA AAGTTAAAGA GAAAATAAGA CCTCGAAATC CTAGCCCCCT AAGAAGAGGC 840
CAAACTGGCC CCACTTTGAG CCTTTCCAGT TCTGATTTGG GCCCAGGGTG GGGAAAAAAG 900
CAAAAGAGAT GGGCACATAG TGCCTGAAGG TGACAGGAAG AGACAGACAA TGCTGGGGCA 960
AACTTGGCAG GCTCCCCAGT GTCACCTTGT GCCCATCCTC AGGGCCACTG CAGCCCCATG 1020
CCGGGGTGGA GGGACTTCCT GTCGGGTGCT GCCGTGGTGG GAGCTGTGTT CCAAGGGCAC 1080
TTAGCGGGTA GGGCAGTCAC CCGGAGTCTG ACTCACCCTG AAGATGGAGT GATAAGAAGT 1140
GAGCTGAACA CCACCATGCC TGGGACCAGA AACTGCACAG ATCTCTACTG CCCAGAGACT 1200
GGCAGGGGGA AAGGGGGAGA GACTCTGCTT CTCCTGGGCA GGCTGAGATC TCGTCAGGCT 1260
GCAGAGCTCC TCACTCTGGG TCCCCTGCAC TCAATGTGCT GCTAGGATGA CTTGGTCCGA 1320
GTATCCACTC TATCTGCTGA CCAGACCAAG AGTTCCTAGA GGGCAGACGT TTGTTGTACC 1380
AGTTTGCACC CACAGGCCTG ACACCAACTA CAGCAGGCAC AGCACTGTGG TAGAGGAGTG 1440
CACAGGAGCG GGGAAATCCC AGCTCCATTT CATCTTGGCT GTGTGACCTT GGGCAAGTTA 1500
TATGACCTGT CTGGCCTCAG TTTCCTCATC TACAAAAATG AGGATAATCA TACTGACATC 1560
ATATCACCAT TACAAGGAAA TGATGAAGGA GAAAAGCCTG CAGCTTAGGG AGCCTGAAGA 1620
ACAGGGAGAA TCAGGCCAGG GCAGGAAGGA AAGGGCTGCA GAAAAGCCAG CGGGGCACAG 1680
GCCCAGAACG GTGTGCCTCT GCAGAGGTCA TGGGAAGCTC CCATGCCCAT CATCCTTATC 1740
AGATGTTCTC AGCAATCCTG TAAGCAGACA GGGCAGTGTT GTAATACCTG CTTCACCAAG 1800
ACATTAGGAG ATGACGTCAG ATGATCTGTG CAGTGTAGAC AGATCTGATT CCCCATTCAG 1860
TGCTTCACCA AGAGTCAGCA GGAACAGGTG GTGACTACCA TCCAAGAGGC TGGGATTAGC 1920
TAAGAGCCAC TGCTCTCCTG TGGGTTCATG TGTTCCCTAA AGGCTTCTGA GCAGAGCAAG 1980
AACAAAGCGC TGAGCGGGAG GCTGGGAGAA CAGCGAGGCT AGAGATAAGG ACTGGAGATA 2040
AGGACGGGAA CTAGGTCAAC AGCGGTGGAC TAGAACAAGG AGGTGCCTCA ACGCTGTGGG 2100
GAGACAGGGA GGAGCAGAAA CAACTGAGGT TCTGCTGGTG ACTCACTGGG GGAAGGAAGG 2160
CGCCTTTGAC AAAAAGGTGG TGGCACTTAG GGGACAAAGA GAAAGGGTGT GGCAGCCTTC 2220
AGGCATTCTA ACGGTGAGGC TTGACACCCA AGGCCTGACG AAGGTTGGTG CCAAGGGATA 2280
GCACCTGTCA AGGTGCCCTC AGCGGTGGAA AGGAGGGCCC GCTCCACTCA GAAGAGAGGC 2340
ACGCTGGGCC CCACCATCCA TATGGCACCT CAAGGGCCAG GCCACGGCAT GCCTAGTGCA 2400
GCTCCTCGCC AGGCCCGTCA CACGGCCCTG CCCAGATATC CTCCATGTGT CTGTCAGGAG 2460
TGTGGGGAGC CAGCCCAAGT CAACTCTGAT CCTATTCTTG CTGCAAGTGC TCAAGGGAGG 2520
CACTACAGAG CTCCTCCAGC AGACTTTATC AGTCGACAAA TACTGACTGG CTCCCCTGTG 2580
GTACTCCATG CTGTACTCAG ATACTCCATG CTGGGTACTG AGGAGGAAGA GGAACGAGTA 2640
GGCACCTAGT GCCCACAGAG CAGGGCAGGG GTTCTTATCC TCGGTGCACA GATTCCAGAG 2700
GTCAATGACC AGACAGAAAC ACAGGCGAGT GTGAGAAGGT GAATCTTAGT GGATGAGAAA 2760
TCTGGAGCTC TTCAGATTCT CAAGGGGGTG GTGACCCACA GGGGAAAAGG GAAGGTGTCA 2820
ACAGCCAGGG AAGGCAGTGT TTTTTTGGGT GGCATTAAGA GGTGTCTACA GAGGCTTTCC 2880
AAAGGAAGTG TCACCTTAAA GGATGAGTGA CAGTGGGGAC AGAGGGACGG AGGGGGAAGA 2940
GAGCAGAGGG AACAACCAGA ACCATTAGTA TGCAAAAGGC CCCTCCCACT GCCCTGAGAC 3000
TTCACCCACA CTGGCCCCAG CAGGAAATAA CCTCTTGAAA GGTCACACAG AGGGCAGGGC 3060
AAAGACCAGT CTCTTCCCCT TCCTTCATAT GCAGCCAGAC TGGACGAGTT CCTCTGGGAA 3120
GTCTGGCCTG GCTCCAAACT CCCTCCAGGG TCCTCCCTGT AGGGGCACTG TGGTATGCAG 3180
GAAGCCCAGC CTGCAGCCCT GGACTGGGCA GGTGGTGGGA ACATCAGGAC ACACTGCTTA 3240
CCAGTGGTGG GACCTCCCTG AGGCTCTGTC TCCTCCCCTG TCAAAGTGGG GCTGGCACTA 3300
CTTTAACAGG GGCATGTGAG GATTATACAA GGCAACTTGG GTCCACCATG TGGTACAGGG 3360
TCCCGCATGA CCCTGCACCA TGAAAAACTG CCTGCTGGCC GGGCACAGTG GCTCACGCCT 3420
GTAATCCCAG CACTTTGGGA GGCCAAGGCA GGTGGATCAT AAGGTCAGGA GTTCGAGACC 3480
AGCCTGGCCA ATATGGTGAA AACCTATCTT TACTAAAACT ACAAAAATTA 3530