EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS149-00652 
Organism
Homo sapiens 
Tissue/cell
NKC 
Coordinate
chr19:45954160-45956280 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RUNX1MA0002.2chr19:45955028-45955039TTCTGTGGTTT+6.32
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_01498chr19:45954229-45954756Adrenal_Gland
SE_02108chr19:45954302-45955473Aorta
SE_02406chr19:45953198-45955557Astrocytes
SE_03036chr19:45954209-45955454Bladder
SE_06640chr19:45954107-45955460Brain_Hippocampus_Middle
SE_09930chr19:45952902-45955562CD14
SE_11261chr19:45952741-45956092CD20
SE_12309chr19:45951605-45955520CD3
SE_13038chr19:45954197-45955074CD34_Primary_RO01480
SE_14395chr19:45951822-45956053CD4_Memory_Primary_7pool
SE_16220chr19:45953121-45955437CD4_Naive_Primary_7pool
SE_16563chr19:45952087-45955902CD4_Naive_Primary_8pool
SE_17214chr19:45954122-45955478CD4p_CD225int_CD127p_Tmem
SE_19219chr19:45953071-45955358CD4p_CD25-_Il17p_PMAstim_Th17
SE_20014chr19:45951268-45955864CD56
SE_20748chr19:45951956-45955882CD8_Memory_7pool
SE_21766chr19:45952843-45955379CD8_Naive_7pool
SE_22333chr19:45951246-45955750CD8_primiary
SE_23143chr19:45953144-45955295Colon_Crypt_1
SE_23745chr19:45953196-45955335Colon_Crypt_2
SE_23745chr19:45955584-45956022Colon_Crypt_2
SE_24769chr19:45953219-45955396Colon_Crypt_3
SE_26771chr19:45951321-45956107Esophagus
SE_29756chr19:45954235-45955480Fetal_Muscle
SE_31887chr19:45953232-45955295Gastric
SE_34472chr19:45953048-45954483HCT-116
SE_35967chr19:45949310-45955744HMEC
SE_38090chr19:45951841-45955296HUVEC
SE_41239chr19:45953511-45955306Left_Ventricle
SE_44217chr19:45953110-45955478NHDF-Ad
SE_44830chr19:45953087-45955467NHLF
SE_45809chr19:45952912-45956134Osteoblasts
SE_47661chr19:45954215-45955058Pancreas
SE_48343chr19:45954170-45955149Psoas_Muscle
SE_49047chr19:45953233-45955712Right_Atrium
SE_50737chr19:45953113-45955920Sigmoid_Colon
SE_51420chr19:45953217-45955529Skeletal_Muscle
SE_52836chr19:45954162-45955472Small_Intestine
SE_53558chr19:45953046-45955367Spleen
SE_57973chr19:45954212-45954605VACO_9m
SE_64393chr19:45949302-45955334NHEK
SE_65504chr19:45953453-45955007Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194595490545955186
Enhancer Sequence
CCCACGCCCG CGCAGACGCG GTGACGCGAC GGACTGTGGA ACGCCGTCGC CTAGCAACGC 60
GAGGGCTGTT TGTCCCGGGC TGGGTGGCGC GGCCGCACAG GGCGCAGCCA GGACCGGCCC 120
GGGCGGACAG ACCGGCCCGC CGGGAGCCCG GGGCGGGGGG TGGAGGGGAT TGCGGTGATG 180
GAAGCGGGGG AGAACCGGGT TCCCAAATTA CCGGTTTCCC TTTAGACAGC CGCCGTCTGT 240
TGTCGCCCGC TCCTCCTGTC TGCCCCGGGA CCGCCTCCGC TCGGGTATCT GTCCGTCTGC 300
GCCCCCTCCT CCCCGGCATG TCCGTCTGTC CAGCGCCTCC CGCGCTGTGG CTGTCTCATA 360
TCCCCCCCAA ACCATCACAA CCAAAATAGG GACAAGCACA CACTTCGCTG GCCTGCCGTT 420
TCTGCCTTGG ACTGCCGGAT TTCCGGGTGC ATTGTTGCGG TTGGGGTCCC CACCAGGGGA 480
GACAGACAGA CAAGGGGAGA CAATCTGTTC ACACTCAAGC CACAGCCCCA AAGCCCTCCC 540
GTTCCTTTCC CCGCTCCCTT GGGGTTCTCT TGCCTGTCTT TCTCGAGCCT CTTTCAAGAG 600
ACAGGCAGCC CGTGGTCCTT CCATCCTGTG TCCGGGAAGC TGTCCACAGC TGGGAGGTTC 660
TAACAACTCA TCCCCAACAC ACACTCCCAA CACCCCCCCA TCCAGTAGCT TCATGTGACC 720
AGGGCTGGGG CGAATCTCCG AGCAGAGAGA AGAAATTGAG TGTGTGACAG TGTGAATGGA 780
TGTGACTATA GGTGAGCAAC AGTCGGTGAC AATGTGCACA TCTGGTATTT CCTGTGTGAG 840
AGCAAAACTG CAGGACTCAG TGAGTGGTTT CTGTGGTTTG CACTTGTGTA TCTGGGTGTA 900
TGGGAGTGTG TAGCCCTGCT GACTGTGTAG ATATGAATGT GTGTGCAGTT GTGAGTCTTG 960
CATGTGGTCA TCTATGTGAA ACAATGCCTG TATAAGTACC CATGGATGTG CACGGTTTTG 1020
CCTCTAGCCG TGCATTTCTG GTTCTGTGTG TGTGTGTTTC TGGTTTTTTC GTTTGTTTTT 1080
TAGAGATGGG GTCTGGCTGT GTTGCCCAGG CTAGTCTTAA ACTCCTGGGC TCAAGCGATC 1140
CCCGCCGTCT CAGCCTCCCG ACTAGTGGGG ACTACAGGCA AGCGCCACTA CACTCGGCTA 1200
ATTTTCTGGT TTTTTTTGTA GAGACAGGAT CTTGCTGTGT TGCTCAGGCT GGTCTCCAAT 1260
TCCTGGCCCC AAGTGATCCT CCCACCTCGG CCTTCCACCA CAGTGCTAGG ATTATAGGCA 1320
TGAGCCACCG TGCCTAGCCA TGTGTGTTTC TGGATTTCTG TGTGTAACCA TGCAGGTACC 1380
TGCGTTTGTG TACAGATTAT TTTTCAGAGC TCCCTCCACA GCATTCATTG CAATGTCTAA 1440
TTATATATTT GTTCCTTTGT TTACTGTCCA TCTCCCCCAC TGGACTGTGC ACCCTGTGAG 1500
GGCAGGACCC AAGGCTGTTG TGGTCACTGC CAGGTCCCCA GCACCACCCT GCACAGAGAA 1560
GGTGCTCAGT AATTCCTTGT TGGGTAAATG AATCGATGAC TCTTATGTCC ATGTCGAGCA 1620
CACACATCCA TGTAACCCTG CAAGTGATTT TGTGGTACTG GGTCTTCTGT GTGTGTCTAG 1680
AAGCTGCGTG GGCCATAGCA CAGGAGGGTC TCTGTAGCCA TGTAGCTCTA ATTTTTGGCA 1740
CCCCCCACAG TGCAGGGCAC ATATCAGAGC CTCATGGCAC ATATCAGGGC CACGTGGAGT 1800
AGGAGGCCAG GTGCACTGGC TCACACCTGC AATCCCAGCA TTTTGGGAGG CTAAGGCAGG 1860
AGGATCACTT GAGACCTGGA GTTCAAGACC AGCCTGGGCA ACAAGGTGAG ACCCTGTCTC 1920
TACACATAAT ACAAAAATTA GGCCAGGCGC AGTGGCTCAT GCCTGTAATC CCAGCAATTT 1980
GGGAGGCCAA GGAGGGTGGA TCACCTGAGG TCAGGAGTTC GAGACCAGCC TAGCCAACAT 2040
GGTGAAACCC CATCTCTACT AAAAATAAAG AAAAAAAAGC CAGGCATGGT GGTGGGTGCC 2100
TGTAATCCCA GCCACTTGGA 2120