EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS087-10302 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr19:4374060-4377010 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr19:4376254-4376265CATGAGTCACC-6.62
FOSL2MA0478.1chr19:4374747-4374758CTGAGTCACCC-6.02
JUNBMA0490.1chr19:4374747-4374758CTGAGTCACCC-6.02
JUNDMA0491.1chr19:4376254-4376265CATGAGTCACC-6.02
NFE2L1MA0089.2chr19:4374761-4374776AGGTGACTCAGCAGT+6.66
ZEB1MA0103.3chr19:4375085-4375096CCCACCTGCCC+6.14
Number of super-enhancer constituents: 33             
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_12725chr19:4373541-4375388CD34_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: 3             
ChromosomeStartEnd
chr1943741094374366
chr1943765374376952
chr1943757354376107
Number: 1             
IDChromosomeStartEnd
GH19I004367chr1943674374382197
Enhancer Sequence
CGGCAGCGAG CCGATGTCAT TTGAAGTCAC AGCACATGAA AATGAGGGGG AGAAAAAAAC 60
TTAGGCAAGA GAAATCCTCC AGATGGGCCC TGGAGGCCCC ATCCAAGAGT CTGAGGCCAA 120
CACATCAGGG GAACTGGAAG CAGAGAGGGA ATCAGCCACT GGAAAGAAGT CACGCAGACG 180
AAGTGGTGAC AGCCACGACA GGAAATTGCT CAGCGGTGGC CACAACAGAG TGGCAGCCAG 240
GGGCCAGGGG CCAGCTCTGT GACCATCCCC GAGAGAGAAA GGGGACATTC AGGCCTGGTC 300
TATGATGGTC TGGTGGCCGG AGGCTCCGTG AGGGCAGCCC CAGGGCCAGA AGGACCTCTC 360
CTGTGCTGAC AGCAAAGTCA CCAGCGGGAG TCCAGCCCAC ACTGCCTTTC TGATGAGGCC 420
TCCAGCTCTG GCTGCTGACT TTAAACCCTA AGGAACCCTG TGCAGGGCCT GCATCCCGGA 480
AGGCCTCCAC CAGCCCGAAC CTGGCCCGTC CGCCCTAGAT GGGGCAATCG GCGTTTCTCC 540
CGGGACAGCC TCCTCCCTGG CCTCCTGGCC CTCGTCTGCA TTGAGAGGCT TGGCCTCTGG 600
TCCGCATGCT GCCCTTCCCG TGCTGTGGCC TTGCAGCCCG GCCTCTCCCC TGCTGTCCCC 660
CTTGGCTCTG GCCTGGCCCC TGGGCCCCTG AGTCACCCCT GAGGTGACTC AGCAGTCCTT 720
GGAAACGCAT GCCGAGGACG CACCCTGCCT GGCCCAGCTC CACATGGGTG TGGGGGAGGC 780
TGCGGGCTGC GCCTGGTGGC CGTATGGGGC CTAGGCTGGC CAGTGCTGCC CAATGGTGGG 840
GGCTCCCTCA CCGCCCGTCT GGCAGAAGCC ATGGGCCACA CGCTGTCCCA GCACATGGTG 900
GCAGGGCGGT GACCTGGGCT CGGCTCTAAT GACCGGCAGC CCTGGGGCTC CCATCACCAC 960
TACCAGTCTG CCCAGGAGGC AGCAGAGCAC TGAGCCCGAC CTGCTCCCCT CGGGCACCTA 1020
CGAGACCCAC CTGCCCCTCC ATGCGTGGGG GAGAAGGGGT GCCCTCTGCT GTGGAAAGCT 1080
GGGACCTACT GTCTGTGGTG CGAGGCTGAC CCCACAGAGC TCCAGGACAA CCCCGAGAGG 1140
AGTGGACAGA GCCAGCCGGG CCCTCCAGCC CCCACCTGGC CCAGCTGCCG CCTCTGGGCA 1200
GATGTCTCCA CTTGATAAAC AGGACAGCTA AGGGCCTAGG AGAGACATGC CTGGCCCAAG 1260
GCCAGACAGC AGGAGTGGCT AGGAAGGTCA AGGGATCCCC ACTGCAGGCC CCACCAACCC 1320
TGGCTCTGCC TGGAATGCAG TCAGGGCAGG TGGAAGGGGA GGGGCAACGC CCCAGGGCTG 1380
GGCGAGGAAT CTGGGAGCAG GTGGGAAGCT CATGCTACCT TCCCAGGAGA CGGGAGGACA 1440
GGCCTGCCAA CCAGGGGGCT CAGCTATGTG GGACACACGC TCCCACCCTT GCCCTTGCAC 1500
AGGGTTTCAT CCAAACATGG AGATGCCAGT GAGTGCCTGG GGCTCCTCTC CCAGGAACAA 1560
ACCACACCCA GAGCTCCAGC CCGAGCGAAC ACATCTACAT GAAAATCAGC CTCATGCATC 1620
ATGCATTGTA ATTTCTCATC TTGGGGACCA GGCAGGAGGG CTGTGTGACA TACAACTGGT 1680
AAAATCAGTT TCCGATGAAA ACTTATAAAA GGAAAAAGCC AACCCACAAA CAAATGAGGC 1740
GATAAATCCC CTGAGGCTCC GCCTGGCAGG GAAACACCAG CTCTGCAGCA CTGAGCACAG 1800
GCTGGTGTTC CCACTGGGGG CAGCATGGAG GATCTGCGTC CAGGGGGCAG AGTGTGATGA 1860
CATCACCCAC ATGCACAGGA ACGATAAGGC TTTCTTAAAA AACGATCTTT TCTCAACAGC 1920
TCCTCAAAAG GAGCTGAGGC AATGCATAGC CCTGCAGGAA GAGACTGGAA ATGGTCTTGG 1980
AGAGAGAACT GCGGGGCATG GTGACAGCGG TGAGAGGCTG CAGGTGCACA GATCTCAACG 2040
AGGGGCCGTG AGTTCCCTCA CTCCCTGAGA GCTGAGGAGA CTTGCCCGAA AGCCCAGAGC 2100
CCTTCCTGAG ACACAGAAAC CATCTTCACC ATCTCTAAGA TCCCTTCCAT TTCTGAAGGA 2160
CTTCCATTTC TTTGTGACTG TGGGCCACCA TGGGCATGAG TCACCTGTCA CCAGAGCCTG 2220
GTGTCCCTGT GCAGCTGTGC CAGGTGGGCA GAGGAGACAG GTGAAGGCAC ATTCCTCAGC 2280
GCCCGCTCAC AGCTCTGCCC ACCGTGCATT CTGTAGAGAA CCTCAGCGCC CTCCTCCCTG 2340
CCGGCAGCCA GGCAGGGATT TAGGTGGTTT CTGTTTGGCC TCCAGTGCTT GCCTCTCCCG 2400
TGTCCTATCC GCCCAGACCT CAGACCTCAG AGAAGCCTCC TCCCACAGGA AGCTCTCCTG 2460
ATTGATCCCC ATCACTGGTC TCCTCACCTT CTCCCAACAC ACCACTGATG CCTCCTCTCT 2520
CGTGCGCCTG CCCCTTCACA CTTCATCTTA CACCCCCATC TGCCTGGGCG GCCCCCCCAT 2580
CTCCCCTCAG AGCTTTTGCT CTCGCTGTTC CTTCTCCCTC ACTGAGCCTC CCTGGATCTT 2640
CCCATGCTGG GTCTTAGCCA CCAGGGCTCT GTCCATCCAA ATGTCCCCAT GGCTGCAAGG 2700
CTGCCCCACC CTCCTGCTAT CCTCACGGGG CCTCGCATTC CTCTTGCTTG CTTGTTTTCG 2760
GGTCCCCTGC TGTCCCGTCT CAGACACAGG AAGCACTCTC CAATGCTTAG CGCCCTAGAA 2820
TAAAGGACCC CGGGCAACCT CTTGGGGGTC CTCGCCACAT CCCACCCCTT GACAGCAGCT 2880
AAGCTCCGGG GGCAGCAACT CCCCGCAGTG ACCCGGAAGG CAGCCAGATG ATACTCCTCC 2940
CATCACCTTC 2950