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

TagContent
EnhancerAtlas ID
HS062-07960 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr19:4063270-4066680 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56356382chr194064057hg19
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr19:4064001-4064013AAACAAACAAAC-6.32
Foxd3MA0041.1chr19:4064005-4064017AAACAAACAAAC-6.32
Foxd3MA0041.1chr19:4064009-4064021AAACAAACAAAC-6.32
KLF16MA0741.1chr19:4065895-4065906GCCCCGCCCCC+6.02
KLF16MA0741.1chr19:4065916-4065927GCCCCGCCCCC+6.02
KLF5MA0599.1chr19:4065895-4065905GCCCCGCCCC+6.02
KLF5MA0599.1chr19:4065916-4065926GCCCCGCCCC+6.02
SP1MA0079.4chr19:4065892-4065907CAGGCCCCGCCCCCT+6.75
SP1MA0079.4chr19:4065913-4065928CTGGCCCCGCCCCCG+6
SP2MA0516.2chr19:4065891-4065908CCAGGCCCCGCCCCCTG+6.27
SP4MA0685.1chr19:4065892-4065909CAGGCCCCGCCCCCTGG+6.48
ZNF263MA0528.1chr19:4066143-4066164CCCACCCCTTCCCCCTCCTTT-6.86
ZNF263MA0528.1chr19:4066190-4066211GCCCCCTCCCCCCCATCCCCC-6.95
ZNF740MA0753.2chr19:4065735-4065748ACCCCCCCCCCAC+6.32
ZfxMA0146.2chr19:4065892-4065906CAGGCCCCGCCCCC-6.19
ZfxMA0146.2chr19:4065317-4065331CAGGCCCGGGCGGG-6.23
ZfxMA0146.2chr19:4064375-4064389GAGGCCCCGGCCCC-6.33
ZfxMA0146.2chr19:4066009-4066023CAGGCCGCGGCGGG-6.91
ZfxMA0146.2chr19:4065639-4065653CCGGGCCCGGCCTG+6
Number of super-enhancer constituents: 64             
IDCoordinateTissue/cell
SE_00556chr19:4056956-4065830Adipose_Nuclei
SE_00903chr19:4057187-4065910Adrenal_Gland
SE_00903chr19:4066063-4068676Adrenal_Gland
SE_02962chr19:4063838-4065740Bladder
SE_02962chr19:4066149-4068642Bladder
SE_03556chr19:4063201-4064827Brain_Angular_Gyrus
SE_04051chr19:4057545-4065617Brain_Anterior_Caudate
SE_04051chr19:4066127-4066786Brain_Anterior_Caudate
SE_04973chr19:4057361-4065386Brain_Cingulate_Gyrus
SE_04973chr19:4066092-4068908Brain_Cingulate_Gyrus
SE_05886chr19:4057056-4065697Brain_Hippocampus_Middle
SE_05886chr19:4066007-4069211Brain_Hippocampus_Middle
SE_06913chr19:4057221-4065787Brain_Hippocampus_Middle_150
SE_06913chr19:4065920-4068916Brain_Hippocampus_Middle_150
SE_07962chr19:4057265-4065433Brain_Inferior_Temporal_Lobe
SE_08937chr19:4064133-4064608Brain_Mid_Frontal_Lobe
SE_09464chr19:4056767-4065799CD14
SE_09464chr19:4065980-4070065CD14
SE_12453chr19:4064215-4065318CD3
SE_12453chr19:4066136-4066635CD3
SE_19502chr19:4062531-4065934CD4p_CD25-_Il17p_PMAstim_Th17
SE_19502chr19:4066111-4068661CD4p_CD25-_Il17p_PMAstim_Th17
SE_20194chr19:4057193-4065599CD56
SE_20194chr19:4066118-4068807CD56
SE_22707chr19:4057277-4065478CD8_primiary
SE_22707chr19:4066170-4068854CD8_primiary
SE_23073chr19:4057648-4065796Colon_Crypt_1
SE_23073chr19:4066126-4068752Colon_Crypt_1
SE_23728chr19:4057699-4065936Colon_Crypt_2
SE_23728chr19:4066076-4068665Colon_Crypt_2
SE_24683chr19:4057638-4068736Colon_Crypt_3
SE_26455chr19:4057364-4065603Duodenum_Smooth_Muscle
SE_26575chr19:4057185-4068797Esophagus
SE_27700chr19:4057184-4065600Fetal_Intestine
SE_27700chr19:4066116-4068829Fetal_Intestine
SE_28696chr19:4057184-4065610Fetal_Intestine_Large
SE_28696chr19:4066096-4068988Fetal_Intestine_Large
SE_31428chr19:4057198-4065934Gastric
SE_31428chr19:4065988-4068833Gastric
SE_41127chr19:4057193-4068832Left_Ventricle
SE_41816chr19:4060130-4065899LNCaP
SE_42412chr19:4057208-4065813Lung
SE_42412chr19:4065941-4068705Lung
SE_47637chr19:4058571-4065806Pancreas
SE_48492chr19:4057155-4065872Psoas_Muscle
SE_48492chr19:4065940-4068707Psoas_Muscle
SE_48938chr19:4057596-4065788Right_Atrium
SE_48938chr19:4065946-4068671Right_Atrium
SE_49728chr19:4063396-4065788Right_Ventricle
SE_50061chr19:4057166-4065809Sigmoid_Colon
SE_50061chr19:4065947-4068805Sigmoid_Colon
SE_52440chr19:4057174-4065796Small_Intestine
SE_53358chr19:4057017-4068784Spleen
SE_55380chr19:4064211-4065764Thymus
SE_55380chr19:4066171-4068236Thymus
SE_56975chr19:4057329-4065896VACO_400
SE_56975chr19:4066113-4068322VACO_400
SE_57558chr19:4063474-4065868VACO_503
SE_58113chr19:4063156-4065868VACO_9m
SE_58113chr19:4066195-4068264VACO_9m
SE_59557chr19:4059049-4078953Ly3
SE_62529chr19:4051126-4090382Tonsil
SE_65287chr19:4057068-4065317Pancreatic_islets
SE_65287chr19:4066027-4067197Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr1940659754066120
chr1940636004063677
chr1940641544064453
chr1940644754064868
Enhancer Sequence
GTCACGGGGC TCATCCAAGG TCGCAGAGCA AGCGTGCCAG CATTCCAACC CTTGAGGAGC 60
CCTCCTTGGA GCATCTGGGC TGCAGTGGGC TGGCTCTGGG GAGGTGACCT CGGTCTCCTC 120
TGGTCATAAA ACCCAGAGCC CTGCCCGCCT CTGAGGACCA AGGTGAGACG AGTTTGTGGC 180
TCGGCAGGAT TGCAGAGGGG CCTCGTATGC ACGTGCGCCA GCCAGGGCCT GCCCGGTGAG 240
GCAGGGAGGC GAGAGGGCTG TGGCTCGTGC TGTGTGACCT TGGGAGCCAT GCTGGCCCTC 300
TCTGAGCCTC AATGTCATCT TCGGACACAG GGTTTAATAA GCCTCGGTGA CACTCCATTT 360
GCAGGCAGGT GCCTGCAGTT GAGCCTCTAC TGCCAACCTC CGGCCCTGCT TAAAGACAGG 420
TGGGCAGGCG CCCCTGGGCC ACCACACAGT GGGAGGGGAC TTTGGACAGG CCCCGAGCTG 480
GAAGGATGGA GCACAGGGGG CAGCTCTGAC CCCACCTGAG TGACCTTGGG CCGCTCTCTG 540
CTTCCCCCTA CGCTTCAGTC TCCCCTGCCT AGTACCGGCA CCTGCTCCGA GGCTTGCTCT 600
AACCTCCGGA GTTTCCAGGC TCACATTTGA CCTCCCCTCC CGGCCTTGGT TTCCTCCTCA 660
TATGGCAACG GGGATCTGCC ACCAGGTGGA CCCAGCTATA GGTCAGAGGG ACTCAAGGAA 720
AGAAAAGGAA AAAACAAACA AACAAACAAA CACCCAGCAG GGATTTGTGA TCGCCCCAGG 780
AACCTTTCCG ACCAGGCCCC AGGCTGGGCT CTGCCTCGGC CGCGCCTCAG TCTCCCGCAC 840
AGAGCAAAGG ACCCATCCAC TGCCTGCGGC CGCCCGCGGG CCTCTGCCGA TGCGTGGCTG 900
CCCGCCCGGG CCCAGGTGCT GACTGGCCGC CACGCAGCCA ATCGGAACTG AATAATAAAT 960
ACCCCCCGGA CTGACCCACG AATTAAAATT TCAGTGTCCC GGTTGGCTCT TCTTTCCTTC 1020
CTTAGACTTC GCTTTTCCAG CGGCCGGCTC CTGCCCCCCC TTCTCCCCCA AGCTCTGTCT 1080
CCACAGCGAT GGCTGGTGGT AAACAGAGGC CCCGGCCCCG CCGATAGGTG CTCTCGGGGC 1140
CCCATGGCGG GTGGCCCTCG CGGACAAACG CCCCCGGCCT GAAGCCCTCA GGCCCTGGCA 1200
GCAGCAGGGC TGGGCTTAGG CCTGGCCTGG CCTGGGCCCC TGCCCCAGCC TGGCCTCCCC 1260
GGGACCTCTC CCAGACCAGT TTGCCAATAG GAAGTGATCG GCCGGTGGTG GGGAGGCACC 1320
CCCAGTGTGG GAGCGGCACG CTCAGGGTTA CGCCCTGGTC CAGTTCTGAG GTTGGGGCGG 1380
GGGGCACTGA CACGGAATCC CCACGCCCTC TCCGGAGGCA GCTGGCAGGG AGGTGGGGGG 1440
GCCCACCGAG CCCGCCACCC ATGGGTGAGC CAGGTGGGTG CCGCGGGTGG CAGGGGCACC 1500
AGCACCTCTG TGACTTCCGC CGCCTGACTG GGGGGAGAGG AGTTGCTGCC TCCCCCCGCC 1560
TCGCCGCCAA CTCCTGGCTG CATTCCGCCA ACATTTAGTG GGCGCCGACT GGGTGTCCGG 1620
GCCCGGGTGG ACAGCAACCT CCCGCCGCGG CCCACCGTGC GCCCCCGCCA GCCAGCCCGG 1680
GCAGCGCCTC CCAGAACCCG CAGAGGCCCG GTCCCTGGGG GGGCACCCGC TCCTCCGCTC 1740
CGCTCAGCCC CCAGCCAGGC TCCCAGGCCG GGGGGGCTGG GTCTCCCGCC CGGGAGGTAG 1800
GGAGCGGGAG GGAGGGGGCT GGATCCCACC AGCTCCCCCC TCCCCTGCCC GGGCTCAGGC 1860
TTCGCACGTG GTGGTGGCGT CAAGGGAAAG GAGGGGGGGT CCGGGCCAGA GGAGACGGGG 1920
TCACGCGCTT TGGGGGCGCG GACGGCGGGG ACTGGGGTGC TCTCTCCGCC CCCTCCCGCG 1980
GGTCGGAGCC GGACGGCCGT CCGGGCAGGG CGAGGGGCCA GGCCAGGCCC CCCACCCGGG 2040
GCTGAGTCAG GCCCGGGCGG GGGCAGGAAG CGGCCCCCTC CCCCGCCCCG GCCGCAGCGC 2100
GCGGCCCCCG CCCGGCCCGC GGTCCCCCGC CGCCTCGCCC GCGCGGGGGG CTCCTACCTC 2160
CTTCCCGGGG CAGCGGCGAG GGGGCCCGGC CCCGGCGGCG GCGGTGGCGG CGGCTGCGGC 2220
TGGGCTGGCT CCCTCCGAGG GGCCGGGAGG CGGCAGTGAG CCTGGCCCCG CGCCACCCCC 2280
CGCCGCCGGC GGCCAATCCC CACCCGGGCT GGGGGGAGGG CGATGCAAAT TACCCCGGAT 2340
CTGGGTCCGC CCGCCCGCCT CCCCCACGCC CGGGCCCGGC CTGCGCTAGG CCGCGCATCC 2400
CCGGGCTCGC CTGCACCGCG CGGCCGCCCG GGCCGCCGCC CTCCCCGGGG AGCGCGGGGA 2460
GGGTGACCCC CCCCCCACGG GCGGGGGGCC GAGGGGAGGG GGGCTGGGGA CGGTTACACA 2520
ACCAGGCGGG GAGGGGCCCC GGGGCGGGGA GGGGGCCGGC CCGCGGGCCG CGCAGCCGGA 2580
AGCCGGGACC GCCACCGGCC CCCGGCGAGG GGAGCCCGGC TCCAGGCCCC GCCCCCTGGC 2640
GGGCTGGCCC CGCCCCCGCG CCGCGCCGCG CGATCGGCCC GCGCCCATTG GCTCTCCGGC 2700
CCGCCGCTCA CCGCCCCTCC TCCGCACCGC CCCTACCCGC AGGCCGCGGC GGGCTGTCGG 2760
CGCGGGGCAC CCTGGGACTT GTAGTCCAAG CCGCTTGCCA CCTGCCGGCT GCAAACGGCG 2820
GAGGGACTAC GAAGCCCAGA GGTCCCTGCG GCCCTGCCCG CCCACCCGGA CACCCCACCC 2880
CTTCCCCCTC CTTTCCGAAG CCCCCCTCCC TGTTTTTTCA GCCCCCTCCC CCCCATCCCC 2940
CATGGAGCTC AATCCTGGCC AACTCCAACG TATGCACGCA GCACCGAATA GGCCCCCGGG 3000
GGGCGAGAGC GCCCCTCGTC TTCAGCTGGA AACTTAGCAG GCGACGCGCC CCCCTATCTC 3060
CCCACGCCGG CTCCCCCCAC CCTCAATGCA GCCCTGCTTC CCCTCCCCCG CTCCCCGCGC 3120
GCCTGGGAGC CCCGAAAAGC CATGCACCCG GGTTGGGGGG GGCTGGCGCA CAAGCTCATG 3180
CACTTAGCCC CCAATCCCCC CTTCCCGGGC GGCGCCCCCT CCCCGCGCTC GGGATCCAGG 3240
GCGCCTCCAG CCTCCGGGCA GCTGCCAACC ACCCCTTCCT CTGAAACTTG GGGGAACGTC 3300
CCCGGCTCCC CGGATCTCCC CTTCCCGAGG GGGCAGCGGT GGCCGCAGCG ACCCCCGCCC 3360
GTCCCCGCCC TGCACCCCGT GCCGGGGGCC GCGCCGGGCG CTGACTTACC 3410