EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS110-03419 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr3:46987870-46990860 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs13092573chr346988561hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr3:46989860-46989871AGAGATAAGGA-6.02
NR2F1MA0017.2chr3:46989541-46989554CAGAGGTCATGGG+6.22
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: 5             
ChromosomeStartEnd
chr34698953346989702
chr34698793146988653
chr34698877546989017
chr34698868646990431
chr34698973646990203
Number: 1             
IDChromosomeStartEnd
GH03I046941chr34698304846992889
Enhancer Sequence
TGTCGGGGAA GGAAGTAATG CTTAAACTCA ATTCTAAATG TCCACTGGGG GATTATGAGG 60
CAGCTAAAGA AGGCAGAGCA TTCCTGGGAG TGGTAACTGC CTACAAAGAC ATGAGAGCGG 120
AGCAAGAGCA CTGTCACAGC CTGCAGAGCA GGCCCACATG GCTGGCCCAG CCTCACCTGA 180
TGCTGTCAGG GGCAGGGCTC ACAGGGCATT CCTCCAGCAC CGTGGGAGGG CTGAGCCCAG 240
CATGAGGGCC GACACCCTGA ACGGGCACTG TGGTAGCCTA CAAGATGTGT CATGGGAGGA 300
ACGGGGAAGA CCAGAAGTCA GGTGAGATCC TCCACTCCCA GCCTGGACCT GCCCCAGCCT 360
GCTGCTGTCT GTGTGTCTGT GTTTGGGAGG GGGGTTAAAG TTAAAATGAG GGCTGGGAAC 420
TGTCACTGGG GGCGGGTGTG CCGAAGCAGG AGGACTTGAG TTCAGGGGAT GAGGAATAAG 480
CCCCTCCCTC TCCCTAAGAC TTCCCAAGGA CTCAAACTTT TAGGAGCTGC TGACTAGAGC 540
TCTCCCTTCC AGAAGGAAAT AAGAGAAGCA GGAAAGGGTT AAGAGAGAGA CATTCAACTT 600
CTCATCTAGG GTCTTCCCAC CCTTCTTTAG CTTCCTGAAG AAGCTAGAGA CTCACCAGGA 660
ACTCATGGGT ACAGAAACAC TTTCCAATCC CCAGGTGATA TGCCCCATTA GCTCTGAGTA 720
CGCCTGCTAT AATGTCCATG GGAAACTGCC CTCTGTTCAA AAGTTAAAGA GAAAATAAGA 780
CCTCGAAATC CTAGCCCCCT AAGAAGAGGC CAAACTGGCC CCACTTTGAG CCTTTCCAGT 840
TCTGATTTGG GCCCAGGGTG GGGAAAAAAG CAAAAGAGAT GGGCACATAG TGCCTGAAGG 900
TGACAGGAAG AGACAGACAA TGCTGGGGCA AACTTGGCAG GCTCCCCAGT GTCACCTTGT 960
GCCCATCCTC AGGGCCACTG CAGCCCCATG CCGGGGTGGA GGGACTTCCT GTCGGGTGCT 1020
GCCGTGGTGG GAGCTGTGTT CCAAGGGCAC TTAGCGGGTA GGGCAGTCAC CCGGAGTCTG 1080
ACTCACCCTG AAGATGGAGT GATAAGAAGT GAGCTGAACA CCACCATGCC TGGGACCAGA 1140
AACTGCACAG ATCTCTACTG CCCAGAGACT GGCAGGGGGA AAGGGGGAGA GACTCTGCTT 1200
CTCCTGGGCA GGCTGAGATC TCGTCAGGCT GCAGAGCTCC TCACTCTGGG TCCCCTGCAC 1260
TCAATGTGCT GCTAGGATGA CTTGGTCCGA GTATCCACTC TATCTGCTGA CCAGACCAAG 1320
AGTTCCTAGA GGGCAGACGT TTGTTGTACC AGTTTGCACC CACAGGCCTG ACACCAACTA 1380
CAGCAGGCAC AGCACTGTGG TAGAGGAGTG CACAGGAGCG GGGAAATCCC AGCTCCATTT 1440
CATCTTGGCT GTGTGACCTT GGGCAAGTTA TATGACCTGT CTGGCCTCAG TTTCCTCATC 1500
TACAAAAATG AGGATAATCA TACTGACATC ATATCACCAT TACAAGGAAA TGATGAAGGA 1560
GAAAAGCCTG CAGCTTAGGG AGCCTGAAGA ACAGGGAGAA TCAGGCCAGG GCAGGAAGGA 1620
AAGGGCTGCA GAAAAGCCAG CGGGGCACAG GCCCAGAACG GTGTGCCTCT GCAGAGGTCA 1680
TGGGAAGCTC CCATGCCCAT CATCCTTATC AGATGTTCTC AGCAATCCTG TAAGCAGACA 1740
GGGCAGTGTT GTAATACCTG CTTCACCAAG ACATTAGGAG ATGACGTCAG ATGATCTGTG 1800
CAGTGTAGAC AGATCTGATT CCCCATTCAG TGCTTCACCA AGAGTCAGCA GGAACAGGTG 1860
GTGACTACCA TCCAAGAGGC TGGGATTAGC TAAGAGCCAC TGCTCTCCTG TGGGTTCATG 1920
TGTTCCCTAA AGGCTTCTGA GCAGAGCAAG AACAAAGCGC TGAGCGGGAG GCTGGGAGAA 1980
CAGCGAGGCT AGAGATAAGG ACTGGAGATA AGGACGGGAA CTAGGTCAAC AGCGGTGGAC 2040
TAGAACAAGG AGGTGCCTCA ACGCTGTGGG GAGACAGGGA GGAGCAGAAA CAACTGAGGT 2100
TCTGCTGGTG ACTCACTGGG GGAAGGAAGG CGCCTTTGAC AAAAAGGTGG TGGCACTTAG 2160
GGGACAAAGA GAAAGGGTGT GGCAGCCTTC AGGCATTCTA ACGGTGAGGC TTGACACCCA 2220
AGGCCTGACG AAGGTTGGTG CCAAGGGATA GCACCTGTCA AGGTGCCCTC AGCGGTGGAA 2280
AGGAGGGCCC GCTCCACTCA GAAGAGAGGC ACGCTGGGCC CCACCATCCA TATGGCACCT 2340
CAAGGGCCAG GCCACGGCAT GCCTAGTGCA GCTCCTCGCC AGGCCCGTCA CACGGCCCTG 2400
CCCAGATATC CTCCATGTGT CTGTCAGGAG TGTGGGGAGC CAGCCCAAGT CAACTCTGAT 2460
CCTATTCTTG CTGCAAGTGC TCAAGGGAGG CACTACAGAG CTCCTCCAGC AGACTTTATC 2520
AGTCGACAAA TACTGACTGG CTCCCCTGTG GTACTCCATG CTGTACTCAG ATACTCCATG 2580
CTGGGTACTG AGGAGGAAGA GGAACGAGTA GGCACCTAGT GCCCACAGAG CAGGGCAGGG 2640
GTTCTTATCC TCGGTGCACA GATTCCAGAG GTCAATGACC AGACAGAAAC ACAGGCGAGT 2700
GTGAGAAGGT GAATCTTAGT GGATGAGAAA TCTGGAGCTC TTCAGATTCT CAAGGGGGTG 2760
GTGACCCACA GGGGAAAAGG GAAGGTGTCA ACAGCCAGGG AAGGCAGTGT TTTTTTGGGT 2820
GGCATTAAGA GGTGTCTACA GAGGCTTTCC AAAGGAAGTG TCACCTTAAA GGATGAGTGA 2880
CAGTGGGGAC AGAGGGACGG AGGGGGAAGA GAGCAGAGGG AACAACCAGA ACCATTAGTA 2940
TGCAAAAGGC CCCTCCCACT GCCCTGAGAC TTCACCCACA CTGGCCCCAG 2990