EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-13470 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:4374140-4376390 
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: 36             
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_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
AGATGGGCCC TGGAGGCCCC ATCCAAGAGT CTGAGGCCAA CACATCAGGG GAACTGGAAG 60
CAGAGAGGGA ATCAGCCACT GGAAAGAAGT CACGCAGACG AAGTGGTGAC AGCCACGACA 120
GGAAATTGCT CAGCGGTGGC CACAACAGAG TGGCAGCCAG GGGCCAGGGG CCAGCTCTGT 180
GACCATCCCC GAGAGAGAAA GGGGACATTC AGGCCTGGTC TATGATGGTC TGGTGGCCGG 240
AGGCTCCGTG AGGGCAGCCC CAGGGCCAGA AGGACCTCTC CTGTGCTGAC AGCAAAGTCA 300
CCAGCGGGAG TCCAGCCCAC ACTGCCTTTC TGATGAGGCC TCCAGCTCTG GCTGCTGACT 360
TTAAACCCTA AGGAACCCTG TGCAGGGCCT GCATCCCGGA AGGCCTCCAC CAGCCCGAAC 420
CTGGCCCGTC CGCCCTAGAT GGGGCAATCG GCGTTTCTCC CGGGACAGCC TCCTCCCTGG 480
CCTCCTGGCC CTCGTCTGCA TTGAGAGGCT TGGCCTCTGG TCCGCATGCT GCCCTTCCCG 540
TGCTGTGGCC TTGCAGCCCG GCCTCTCCCC TGCTGTCCCC CTTGGCTCTG GCCTGGCCCC 600
TGGGCCCCTG AGTCACCCCT GAGGTGACTC AGCAGTCCTT GGAAACGCAT GCCGAGGACG 660
CACCCTGCCT GGCCCAGCTC CACATGGGTG TGGGGGAGGC TGCGGGCTGC GCCTGGTGGC 720
CGTATGGGGC CTAGGCTGGC CAGTGCTGCC CAATGGTGGG GGCTCCCTCA CCGCCCGTCT 780
GGCAGAAGCC ATGGGCCACA CGCTGTCCCA GCACATGGTG GCAGGGCGGT GACCTGGGCT 840
CGGCTCTAAT GACCGGCAGC CCTGGGGCTC CCATCACCAC TACCAGTCTG CCCAGGAGGC 900
AGCAGAGCAC TGAGCCCGAC CTGCTCCCCT CGGGCACCTA CGAGACCCAC CTGCCCCTCC 960
ATGCGTGGGG GAGAAGGGGT GCCCTCTGCT GTGGAAAGCT GGGACCTACT GTCTGTGGTG 1020
CGAGGCTGAC CCCACAGAGC TCCAGGACAA CCCCGAGAGG AGTGGACAGA GCCAGCCGGG 1080
CCCTCCAGCC CCCACCTGGC CCAGCTGCCG CCTCTGGGCA GATGTCTCCA CTTGATAAAC 1140
AGGACAGCTA AGGGCCTAGG AGAGACATGC CTGGCCCAAG GCCAGACAGC AGGAGTGGCT 1200
AGGAAGGTCA AGGGATCCCC ACTGCAGGCC CCACCAACCC TGGCTCTGCC TGGAATGCAG 1260
TCAGGGCAGG TGGAAGGGGA GGGGCAACGC CCCAGGGCTG GGCGAGGAAT CTGGGAGCAG 1320
GTGGGAAGCT CATGCTACCT TCCCAGGAGA CGGGAGGACA GGCCTGCCAA CCAGGGGGCT 1380
CAGCTATGTG GGACACACGC TCCCACCCTT GCCCTTGCAC AGGGTTTCAT CCAAACATGG 1440
AGATGCCAGT GAGTGCCTGG GGCTCCTCTC CCAGGAACAA ACCACACCCA GAGCTCCAGC 1500
CCGAGCGAAC ACATCTACAT GAAAATCAGC CTCATGCATC ATGCATTGTA ATTTCTCATC 1560
TTGGGGACCA GGCAGGAGGG CTGTGTGACA TACAACTGGT AAAATCAGTT TCCGATGAAA 1620
ACTTATAAAA GGAAAAAGCC AACCCACAAA CAAATGAGGC GATAAATCCC CTGAGGCTCC 1680
GCCTGGCAGG GAAACACCAG CTCTGCAGCA CTGAGCACAG GCTGGTGTTC CCACTGGGGG 1740
CAGCATGGAG GATCTGCGTC CAGGGGGCAG AGTGTGATGA CATCACCCAC ATGCACAGGA 1800
ACGATAAGGC TTTCTTAAAA AACGATCTTT TCTCAACAGC TCCTCAAAAG GAGCTGAGGC 1860
AATGCATAGC CCTGCAGGAA GAGACTGGAA ATGGTCTTGG AGAGAGAACT GCGGGGCATG 1920
GTGACAGCGG TGAGAGGCTG CAGGTGCACA GATCTCAACG AGGGGCCGTG AGTTCCCTCA 1980
CTCCCTGAGA GCTGAGGAGA CTTGCCCGAA AGCCCAGAGC CCTTCCTGAG ACACAGAAAC 2040
CATCTTCACC ATCTCTAAGA TCCCTTCCAT TTCTGAAGGA CTTCCATTTC TTTGTGACTG 2100
TGGGCCACCA TGGGCATGAG TCACCTGTCA CCAGAGCCTG GTGTCCCTGT GCAGCTGTGC 2160
CAGGTGGGCA GAGGAGACAG GTGAAGGCAC ATTCCTCAGC GCCCGCTCAC AGCTCTGCCC 2220
ACCGTGCATT CTGTAGAGAA CCTCAGCGCC 2250