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

TagContent
EnhancerAtlas ID
HS197-10702 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr19:39196770-39198750 
Target genes
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZEB1MA0103.3chr19:39196827-39196838CCCACCTGCCC+6.14
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00117chr19:39197743-39199485Adipose_Nuclei
SE_00865chr19:39195519-39196974Adrenal_Gland
SE_00865chr19:39197223-39205990Adrenal_Gland
SE_01543chr19:39194086-39205969Aorta
SE_03166chr19:39196433-39197174Brain_Angular_Gyrus
SE_03166chr19:39197894-39199452Brain_Angular_Gyrus
SE_03903chr19:39197211-39205540Brain_Anterior_Caudate
SE_04868chr19:39195321-39206058Brain_Cingulate_Gyrus
SE_05805chr19:39182078-39206004Brain_Hippocampus_Middle
SE_06803chr19:39195820-39205439Brain_Hippocampus_Middle_150
SE_07777chr19:39194039-39206085Brain_Inferior_Temporal_Lobe
SE_08790chr19:39197897-39198156Brain_Mid_Frontal_Lobe
SE_08790chr19:39198408-39199265Brain_Mid_Frontal_Lobe
SE_09404chr19:39197597-39198685CD14
SE_23062chr19:39197311-39199581Colon_Crypt_1
SE_23732chr19:39197344-39197714Colon_Crypt_2
SE_23732chr19:39198450-39198762Colon_Crypt_2
SE_24739chr19:39197294-39197869Colon_Crypt_3
SE_26525chr19:39194058-39205949Esophagus
SE_27614chr19:39180632-39201469Fetal_Intestine
SE_28533chr19:39164445-39201888Fetal_Intestine_Large
SE_29583chr19:39197343-39198677Fetal_Muscle
SE_31384chr19:39194037-39199678Gastric
SE_34299chr19:39197188-39198541HCT-116
SE_38012chr19:39197217-39199928HUVEC
SE_40594chr19:39194015-39206697Left_Ventricle
SE_41601chr19:39197275-39199500LNCaP
SE_42097chr19:39194095-39205995Lung
SE_44161chr19:39197660-39199486NHDF-Ad
SE_45660chr19:39196090-39205729Osteoblasts
SE_47114chr19:39164477-39226374Panc1
SE_47461chr19:39197437-39197841Pancreas
SE_48555chr19:39195085-39205958Right_Atrium
SE_49449chr19:39197429-39198476Right_Ventricle
SE_50056chr19:39194910-39205530Sigmoid_Colon
SE_51136chr19:39195385-39206359Skeletal_Muscle
SE_52339chr19:39194079-39204831Small_Intestine
SE_53291chr19:39194893-39205783Spleen
SE_54534chr19:39196075-39206175Stomach_Smooth_Muscle
SE_56725chr19:39197411-39199669VACO_400
SE_65266chr19:39195019-39197876Pancreatic_islets
SE_65266chr19:39197900-39206193Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr193919744339197892
Number: 1             
IDChromosomeStartEnd
GH19I038673chr193916453639206516
Enhancer Sequence
GGTAAGCGCC AGTCCTGGTC ATCCTCTCCT TTCCTCTAGG AACCTGAGAT CCTTCCTCCC 60
ACCTGCCCTG TTTGCTGTGT TTTTGTCGTG GTCTGTGAGA TGCCAGCCCT CAGTCAGCCC 120
CTCCCTGGCC ACGGGCCCTA CAAGCCCATG GGAAGGTCAC CTGGTCCTCT CTGAGGAAGA 180
GGAGGCAGTT TCCCAGCCAT CCTGGCTGAA GGCAGTAAGG TCAGCCCTCT CGCCGGCCTA 240
ATAGAACGTT CTTCGTCCCC AGGCAAGGTG ACTCTCAGAA GCAACAATAA AGCTTTTCAT 300
TTTTGAGACA GGGTCTTGTG CTGTCACCCA GACTGGAGGG CAGTGGTGTG ATCACTCATC 360
CCTGCTGCCT TGGCCTAGGC TCAAGTGATC CTCCTGTCTC AGCCTCCCAA GTAGCTGGGA 420
CTGCAGGTGC ATGCAGCCAC ACCTGGCTAA TTTTTAATTT TTATTTTTAG TAGGAACAGG 480
GTCTCCCTAT GTTGCCCAGG CTGGACTTGA ACTCCTGAGC TCAAGCAGTC CTCCTACCCC 540
GGCCTCCCAA AGTGCTGGGA CTACAGATGT GAGCCACTGC CTGCCTCTGG CCTCTTCCTT 600
TATTTTGACA GCTCAGGAGT GAATTGTTTT TAGAATTGCT AGTAAATTTA GTGTTGGGGA 660
AAAATGTACT CTGTGGCTGC TAAGATGAAC AAGCCTCAGC TCCACCATGA ACCTGCTTCC 720
CTCAGGGTGA GCGGGAGATG AGACATGTCC ACCATCCCCG TAGCTGAGGC GAGCATGGGC 780
ACTGCCGCAT GAGGTCCAGG GGGCGGCAAG AGGCAGGCCT GCCTGGTGGT TGGGAGCACT 840
GGCTCTGGGG GCGGTCCTGA GGTCAGATCC GGTTTGCCTT GTGGCTCCAC CCTCTGAGTC 900
TCCTGGATGG CCCGCACAGG AATGAAGAGC AGGGCCTCAT GGGGTTTGCA GCGGCCTCAG 960
GCTCTCTGGG ACCCTTGCTG GGTACAGAGG GCTTTTCCCA TCGTGCTCAC CCTGATAGCA 1020
TGTGGTCCCT CCCTTGGTCA CTCTTCTCTG TGTGTCTTCT TTTTTTTCCT GCCACTAACT 1080
GACTGAATCT TTCTATAGTT TCCATTCATT TTCTTCAACT AGTAAGTATC TAGCATGCCC 1140
GCTGCATGCC GTTAGTGGAG ATACAGTGGC ACCCAAACAA AGTTCCCATT TGTGGGAAGT 1200
TTACACCACA GCGCGGGGAC CAGCTGTTAG CACAGCGGCC AGTAATCCTG CAGCATAACT 1260
TCAGTGAGAA GTGCTGCACA AAGACAGGGA AGTCAGATGA AGAAAGTTCC CTGGGTGGCC 1320
TTTCTGAGGA GGTGACATCG AGCTTGACCT CAGAGGGAAC CAACCCTTAG AGGGTCTCAG 1380
GGAGGAGAAT GTGACCCATA TAGCTTGTAA CTGACCAACT TGTGGCCTTG GGGAAGGTCT 1440
CTTTCCTCCA GAGACCAGCA TGCCAAGTGA AATCCTGGCA TTTAGCCAGC CCACGGACTG 1500
GCCTTCCTGT AAGTCAGGTC CGCCAGGGTG TGGAGGCCAC ACAGCACAAA CACCAGCATC 1560
CTGCAGTGGC CACCTCCCCC GAAGCGGCCT GTCTGGTTCA GGGCGGCCTC CCATGGAAGG 1620
TGCTAGCAGT TATAAAGCAG TTGTCAGGAG TCAGGCACTG ATCCAAGCAT TTACTCATTT 1680
AATCCGCACA ACAGCCCTAT GTAGCAGGTA TGTCACTATC CCCATCATAC AGATGTGGAA 1740
ACCGAGATAG CCTGGCTTAC CCGAGGTCAC ACTGTCAGTA GGCAGAAGAG TCAGGATTTG 1800
ATCACAGACT GCCTGGCCCC AGAGGTCATG CTTGCAGCCT CTCTGCCACA CTGTCTCCAT 1860
GCAGTGCCTG GCACAGGCCA GACTGCAGTG AATGGGAATT AGTCACTGCT GTGGGTGCAC 1920
AGGGCCATAC GGCACTCTCA TGACAGTGAG CGGGCCCTCC TATAACCTTT GCCTTTCCTT 1980