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

TagContent
EnhancerAtlas ID
HS019-07871 
Organism
Homo sapiens 
Tissue/cell
CD20+ 
Coordinate
chr19:4374820-4376640 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr19:4376254-4376265CATGAGTCACC-6.62
JUNDMA0491.1chr19:4376254-4376265CATGAGTCACC-6.02
ZEB1MA0103.3chr19:4375085-4375096CCCACCTGCCC+6.14
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00671chr19:4372603-4377782Adipose_Nuclei
SE_00953chr19:4369010-4378529Adrenal_Gland
SE_03081chr19:4373372-4375693Bladder
SE_05654chr19:4369240-4377898Brain_Cingulate_Gyrus
SE_06216chr19:4367183-4378196Brain_Hippocampus_Middle
SE_08374chr19:4369264-4378128Brain_Inferior_Temporal_Lobe
SE_12525chr19:4374150-4375101CD34_adult
SE_12525chr19:4375113-4375691CD34_adult
SE_12525chr19:4376053-4376297CD34_adult
SE_12525chr19:4376307-4376536CD34_adult
SE_12725chr19:4373541-4375388CD34_fetal
SE_12725chr19:4375391-4375655CD34_fetal
SE_12725chr19:4376134-4376375CD34_fetal
SE_14750chr19:4367713-4381827CD4_Memory_Primary_7pool
SE_26598chr19:4366396-4381720Esophagus
SE_27964chr19:4373020-4377930Fetal_Intestine
SE_28734chr19:4372075-4378347Fetal_Intestine_Large
SE_30332chr19:4367899-4377712Fetal_Muscle
SE_31749chr19:4372054-4378341Gastric
SE_37296chr19:4367503-4381769HSMMtube
SE_38442chr19:4373325-4377704HUVEC
SE_40064chr19:4371892-4377882K562
SE_41739chr19:4374225-4375739LNCaP
SE_41739chr19:4375788-4376658LNCaP
SE_42702chr19:4371440-4378535Lung
SE_44622chr19:4371840-4377656NHDF-Ad
SE_45249chr19:4372679-4376637NHLF
SE_47754chr19:4373974-4376769Pancreas
SE_48336chr19:4367194-4378514Psoas_Muscle
SE_49011chr19:4372055-4378263Right_Atrium
SE_53019chr19:4371950-4378408Small_Intestine
SE_53804chr19:4371474-4376759Spleen
SE_57120chr19:4373475-4378484VACO_400
SE_57934chr19:4373729-4376544VACO_9m
SE_64150chr19:4373205-4378580HSMM
SE_65589chr19:4367712-4380728Pancreatic_islets
SE_69091chr19:4373604-4377851H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1943757354376107
Number: 1             
IDChromosomeStartEnd
GH19I004367chr1943674374382197
Enhancer Sequence
CACATGGGTG TGGGGGAGGC TGCGGGCTGC GCCTGGTGGC CGTATGGGGC CTAGGCTGGC 60
CAGTGCTGCC CAATGGTGGG GGCTCCCTCA CCGCCCGTCT GGCAGAAGCC ATGGGCCACA 120
CGCTGTCCCA GCACATGGTG GCAGGGCGGT GACCTGGGCT CGGCTCTAAT GACCGGCAGC 180
CCTGGGGCTC CCATCACCAC TACCAGTCTG CCCAGGAGGC AGCAGAGCAC TGAGCCCGAC 240
CTGCTCCCCT CGGGCACCTA CGAGACCCAC CTGCCCCTCC ATGCGTGGGG GAGAAGGGGT 300
GCCCTCTGCT GTGGAAAGCT GGGACCTACT GTCTGTGGTG CGAGGCTGAC CCCACAGAGC 360
TCCAGGACAA CCCCGAGAGG AGTGGACAGA GCCAGCCGGG CCCTCCAGCC CCCACCTGGC 420
CCAGCTGCCG CCTCTGGGCA GATGTCTCCA CTTGATAAAC AGGACAGCTA AGGGCCTAGG 480
AGAGACATGC CTGGCCCAAG GCCAGACAGC AGGAGTGGCT AGGAAGGTCA AGGGATCCCC 540
ACTGCAGGCC CCACCAACCC TGGCTCTGCC TGGAATGCAG TCAGGGCAGG TGGAAGGGGA 600
GGGGCAACGC CCCAGGGCTG GGCGAGGAAT CTGGGAGCAG GTGGGAAGCT CATGCTACCT 660
TCCCAGGAGA CGGGAGGACA GGCCTGCCAA CCAGGGGGCT CAGCTATGTG GGACACACGC 720
TCCCACCCTT GCCCTTGCAC AGGGTTTCAT CCAAACATGG AGATGCCAGT GAGTGCCTGG 780
GGCTCCTCTC CCAGGAACAA ACCACACCCA GAGCTCCAGC CCGAGCGAAC ACATCTACAT 840
GAAAATCAGC CTCATGCATC ATGCATTGTA ATTTCTCATC TTGGGGACCA GGCAGGAGGG 900
CTGTGTGACA TACAACTGGT AAAATCAGTT TCCGATGAAA ACTTATAAAA GGAAAAAGCC 960
AACCCACAAA CAAATGAGGC GATAAATCCC CTGAGGCTCC GCCTGGCAGG GAAACACCAG 1020
CTCTGCAGCA CTGAGCACAG GCTGGTGTTC CCACTGGGGG CAGCATGGAG GATCTGCGTC 1080
CAGGGGGCAG AGTGTGATGA CATCACCCAC ATGCACAGGA ACGATAAGGC TTTCTTAAAA 1140
AACGATCTTT TCTCAACAGC TCCTCAAAAG GAGCTGAGGC AATGCATAGC CCTGCAGGAA 1200
GAGACTGGAA ATGGTCTTGG AGAGAGAACT GCGGGGCATG GTGACAGCGG TGAGAGGCTG 1260
CAGGTGCACA GATCTCAACG AGGGGCCGTG AGTTCCCTCA CTCCCTGAGA GCTGAGGAGA 1320
CTTGCCCGAA AGCCCAGAGC CCTTCCTGAG ACACAGAAAC CATCTTCACC ATCTCTAAGA 1380
TCCCTTCCAT TTCTGAAGGA CTTCCATTTC TTTGTGACTG TGGGCCACCA TGGGCATGAG 1440
TCACCTGTCA CCAGAGCCTG GTGTCCCTGT GCAGCTGTGC CAGGTGGGCA GAGGAGACAG 1500
GTGAAGGCAC ATTCCTCAGC GCCCGCTCAC AGCTCTGCCC ACCGTGCATT CTGTAGAGAA 1560
CCTCAGCGCC CTCCTCCCTG CCGGCAGCCA GGCAGGGATT TAGGTGGTTT CTGTTTGGCC 1620
TCCAGTGCTT GCCTCTCCCG TGTCCTATCC GCCCAGACCT CAGACCTCAG AGAAGCCTCC 1680
TCCCACAGGA AGCTCTCCTG ATTGATCCCC ATCACTGGTC TCCTCACCTT CTCCCAACAC 1740
ACCACTGATG CCTCCTCTCT CGTGCGCCTG CCCCTTCACA CTTCATCTTA CACCCCCATC 1800
TGCCTGGGCG GCCCCCCCAT 1820