EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS145-03852 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr10:134231420-134233910 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10781573chr10134233608hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr10:134233872-134233893TGTTCTTCATCTTCCTCCTCT-6.11
ZNF263MA0528.1chr10:134232195-134232216CCTTCCCCTCCTCCCTCCCCG-6.19
ZNF263MA0528.1chr10:134231878-134231899GGGGGAGGGGTCGGGGGAGGG+6.69
ZNF263MA0528.1chr10:134233845-134233866CCTTCTTTCTCTTCTTCCTCT-6.86
ZNF263MA0528.1chr10:134233848-134233869TCTTTCTCTTCTTCCTCTTCC-6.86
ZNF263MA0528.1chr10:134233851-134233872TTCTCTTCTTCCTCTTCCTCT-6.97
ZNF263MA0528.1chr10:134232191-134232212CTCCCCTTCCCCTCCTCCCTC-7.97
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00873chr10:134226770-134236735Adrenal_Gland
SE_02964chr10:134231826-134233017Bladder
SE_02964chr10:134233042-134233655Bladder
SE_04410chr10:134231065-134232866Brain_Anterior_Caudate
SE_04410chr10:134233156-134238501Brain_Anterior_Caudate
SE_09804chr10:134228334-134237697CD14
SE_10426chr10:134229819-134237452CD19_Primary
SE_11568chr10:134228105-134238193CD20
SE_23061chr10:134228659-134236350Colon_Crypt_1
SE_23725chr10:134229390-134236228Colon_Crypt_2
SE_24681chr10:134229263-134236759Colon_Crypt_3
SE_26753chr10:134230541-134237300Esophagus
SE_28153chr10:134231057-134236765Fetal_Intestine
SE_29112chr10:134231073-134236603Fetal_Intestine_Large
SE_31406chr10:134229991-134236773Gastric
SE_33290chr10:134231995-134232554H1
SE_34405chr10:134231475-134236275HCT-116
SE_41567chr10:134228546-134232988LNCaP
SE_41567chr10:134233089-134236216LNCaP
SE_42252chr10:134219499-134237674Lung
SE_47467chr10:134231344-134236211Pancreas
SE_50143chr10:134230102-134237596Sigmoid_Colon
SE_53287chr10:134219205-134237202Spleen
SE_56893chr10:134230770-134236362VACO_400
SE_57427chr10:134231383-134233121VACO_503
SE_57427chr10:134233122-134236042VACO_503
SE_57946chr10:134231417-134233028VACO_9m
SE_57946chr10:134233141-134233411VACO_9m
SE_57946chr10:134233437-134234418VACO_9m
SE_60105chr10:134230766-134267420Ly4
SE_61428chr10:134196155-134334764Toledo
SE_65264chr10:134210665-134236634Pancreatic_islets
SE_68705chr10:134230320-134236371H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10134233193134233800
Enhancer Sequence
CATAGTTGAA GTTGTGACTT GTGCGGCCAC AGTTCACACT CATGCGTGTG TCCCTGTCGG 60
GGCTGACGGG GCCTGAGTCC CCTGGGCACT GCTGGGCGGG GCCCATGTCG TACGGGTTGG 120
GGTGACGCCG CCACCGGCTG CATCTCGCTG CCTCCAGGTG GGGGGACGCT GGTCACCGCC 180
CTGAGCCCCA GGAGGGCTGT GGGCTGAGTC CCCATCTCCA GGCCTCCCTG CTGGCTTTCC 240
AGTGGACGCT GGGATTTCCT GGAGAGGCAG TGCTCTGCAC GCGGGGAGCT TTGTTCTTTG 300
TTTCCTGGAG TGACTCCTCT CATCCCTTGT TTCTTGATTT GCTCATTCAG AACCAAGGGA 360
GATCTCAGAG ATGACGATGG TGGCTTTGCT TGTTCCTGGT TTTGCTAGAA CATTCTGTGC 420
TCTAAAGGCA TCGCTGCCCT CAGCAAGGAT CGTCTGGCGG GGGAGGGGTC GGGGGAGGGC 480
AGCAGCATAC ACCTGGAGGG TCCTCTCCAG GGCACATGAG GGAACAACCC TCATGGTTTC 540
CTATGGTTCT GGACCTGACT TGCGAGGAGG GGCATGGTTT TCAAACTGGT TTGTAGCAGC 600
AGAGCCCTTT TCTCCAACAA AATCACCCAG AATCACTTCC TCCCGGAGGG GCTGGGCTCA 660
TCCTCCTGAA GCCCTCCAGG CCCAAGAGTC CTGGGAAGCC TTTGAAAATC CAGGGAGGGG 720
CTCGCATGAG CCCAGGAGAG CAGAGCCAGG ACTTGAGAGG AATGAGAGCA GCTCCCCTTC 780
CCCTCCTCCC TCCCCGGCCC TGCCCACGTG GGTGCAGCAG AGTCAGGGCC CTGGCCCTTG 840
GGGCTGGGCA TCTCATCCCT CTGAGCTCCG GTGCCCAGGG GCTGCCCCTG CCTGATCTGC 900
TGCTCGGGGT GACTCCCCCT GCCGCACACC CCACTTTGCA CCCAGGACCT CCTACTGACT 960
AGGGTTGGCT CCCCTTTACG AAGGAAGGCC TTCGTAAAGC TTGGCACTGC TTCAAGAAAT 1020
GTGTGTGTCC AATGGAAGGA GCAGGCCTCA CCCCTGGGAC AAAATATGCG TGCAGCCCTG 1080
GGCACATTCA CTCCCAGCTG CCCAGCCTGC AACTAGAGCT CAGCCACTGC AGGTGACAGC 1140
AACGGGACCC GCCTTTGAGC CTGAGGCCAG GACTGACGCC ACAGCCTGCA GCTCCTCCCC 1200
AAGCCCAGCC CCAGCCCTTG CCCTTCAATC CTGAGACCCT GAGATGCATG GGTGGGGCTT 1260
TCATCCGGTG AGGAGCGGAG GCCCAGGGAG GTGGGTTCCC CAGCTGCCAG TACCCACTGG 1320
TCAGGCTGGG CTGGACCAGG TCCTGAATCC CCGCCCTTCC ACCCATGGGC TCCCCAGGAA 1380
GGCTAAACTG AGGGAAGAAT TCCTGCTGGG AAAGCCCTGT TCTGGGACCA GGGTTTCGTC 1440
CCTCTATTAG AGGGGGTCAG GGGGACACCT GGGAGCGGAA CACCTGAGGG AGGAGCACCT 1500
GGCGGGGAGC CTTGGGGGAG GAGGCACCTG GGGGAGGAAG TCTGGAGGAG GGGTCTCCTG 1560
GTGGGGGGCC TGGAGGAGGG GTCTCCTGGG GGAGGGGCCT GGAGGAGGGG TCTCCTGGGG 1620
GAGGGGCCTG GAGGAGGGGT CTCCTGGGGG AGGGGCCTGG AGGAGGGGTC TCCTGGGGGG 1680
GGGCCTGGAG GAGGGGTCTC CTGGGGGAGG GGCCTGGAGG AGGGGTCTCC TGGGGGAGGG 1740
GCCCTTGGGG AGCCAACCCT AGTCAGTACG AGGTCCTGGG TGCAAAGTGG GTTGTGCGGC 1800
AGGGGGCTTG GGGCCTCAGC GGGGCTGCCC GGAGCTGGTC CTGGGCCTCT CTTGCTCTGG 1860
GTCTCCCCTG CTCTGGGTCC AGCCTCCCAA GCACCCCACC TGGCAAGACT TCCTCGCTCA 1920
GAACAGAGCC AACCCTGGCT GTCTTCCCAG GGTTTGTCGT GGAGAGGGCT CTGGCCCTTT 1980
AGCCTTCCAA GGAGCTTTCG GGGTTGGGGT ACGTTTGTGA CCCCAGTAGC CGCTGTGCTG 2040
GGGGCCCAGG GCAACTCCTC CGGGAGCAGG GAAGGCACTG CTGGCACCAC CAGCCCCGCA 2100
GGGTCACCAG CATCCCGTCT CCACCAGGGC TGCTGCTGTC CCTCCTCTGC TGAGGCCAGC 2160
TGTTACCGTG TTCGACATGG ACCAGGCCGT GTGGGAGGAC ACGGGGTGGC AGGTGCAGGG 2220
AGCACGGTCT GTTTTCTGTC ACTCTCTGGT CCCAGCCTGA GCCCCAATCC CTACCTCTGA 2280
GGGTCACACT TCCAACCCAC CCCAGACAGA GCTGGAAGCA GGGGCTGGCA TGGGCGCTGG 2340
GGTAGACGCA GGGGTTGTCG TGGCCTGGCG TGGAAGAGCT GGGCTGGACG CAGTGGGTGG 2400
CGTGGCCTGG GGTGCTGCTC TCCAGCCTTC TTTCTCTTCT TCCTCTTCCT CTTGTTCTTC 2460
ATCTTCCTCC TCTTGCTGCA GATCCTCCCC 2490