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

TagContent
EnhancerAtlas ID
HS068-02709 
Organism
Homo sapiens 
Tissue/cell
GM18526 
Coordinate
chr19:2043930-2046180 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr19:2045780-2045791GGCCACACCCT+6.32
ZNF263MA0528.1chr19:2045516-2045537TCTTCTTCCTCCTTCTCCTCA-7.31
ZNF263MA0528.1chr19:2045510-2045531CACCCCTCTTCTTCCTCCTTC-7.56
ZNF263MA0528.1chr19:2045513-2045534CCCTCTTCTTCCTCCTTCTCC-8
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00410chr19:2040386-2053186Adipose_Nuclei
SE_00877chr19:2043921-2052778Adrenal_Gland
SE_04258chr19:2044008-2046265Brain_Anterior_Caudate
SE_06065chr19:2039897-2052942Brain_Hippocampus_Middle
SE_07327chr19:2044014-2044825Brain_Hippocampus_Middle_150
SE_10185chr19:2040263-2045628CD19_Primary
SE_11386chr19:2039336-2059166CD20
SE_14636chr19:2040442-2045353CD4_Memory_Primary_7pool
SE_17004chr19:2043861-2044867CD4p_CD225int_CD127p_Tmem
SE_17626chr19:2038511-2053432CD4p_CD25-_CD45RAp_Naive
SE_17917chr19:2039716-2046074CD4p_CD25-_CD45ROp_Memory
SE_19564chr19:2044248-2045137CD4p_CD25-_Il17p_PMAstim_Th17
SE_20037chr19:2040265-2045959CD56
SE_22582chr19:2040027-2045973CD8_primiary
SE_23148chr19:2043996-2046324Colon_Crypt_1
SE_23772chr19:2044008-2044451Colon_Crypt_2
SE_23772chr19:2044918-2045894Colon_Crypt_2
SE_26566chr19:2038851-2054518Esophagus
SE_31409chr19:2043840-2053094Gastric
SE_34292chr19:2043816-2045874HCT-116
SE_34839chr19:2044769-2045848HeLa
SE_40728chr19:2042250-2052968Left_Ventricle
SE_41572chr19:2043959-2052890LNCaP
SE_42204chr19:2043982-2052921Lung
SE_47494chr19:2044388-2044885Pancreas
SE_47494chr19:2044892-2046918Pancreas
SE_48086chr19:2036911-2052819Psoas_Muscle
SE_48699chr19:2043842-2046365Right_Atrium
SE_49469chr19:2044029-2044865Right_Ventricle
SE_50075chr19:2043846-2046189Sigmoid_Colon
SE_51187chr19:2038576-2052883Skeletal_Muscle
SE_52407chr19:2043967-2046162Small_Intestine
SE_53798chr19:2037650-2053000Spleen
SE_54890chr19:2044138-2046081Stomach_Smooth_Muscle
SE_55272chr19:2043998-2044619Thymus
SE_59032chr19:2040556-2063003Ly3
SE_59944chr19:2041147-2096724Ly4
SE_60429chr19:2041140-2096762DHL6
SE_65305chr19:2038632-2051258Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1920440002044600
Enhancer Sequence
CCATTGCACT CCAGCATCCT GGTGACAGAG TGAGACTTCG CCTCAAAAAA AAAAAAAAAA 60
AAAAAAAAAA AAAGCCAGTG GAGGCTGCTC TCCACCTGTG ACCCTGACAG CCCTCAGAGA 120
CACATTTGAG ACCTATGACT TCTGCAAAAT ACCCCCACAG GACGTGAGGG TTCCCTGCCC 180
TGGGCGGCCA CCCTCCCTGA CCCAGAGACA GTCAGCTGTA GTCCTCTTTC CCCACAGGGT 240
GGGTACCTGG TCACCCATAG AACTAGGGAG GCCTCAGGAC ACCTGGCTGC CAGCCCACCA 300
GGCCCCACCT CACATGTGGC CACAGCACCA AGTCCTGCTC CCCAGCTCCG TGCCAGCCTG 360
GGCAGACACT TGCCTGCCGC CTCAGCCAAT ATCTGTTTCG GGCCCACCCT GGTTGGCTGT 420
CCCAGCCACT GGCGGATCCA GCCTCCCTGA GCCCCAGAGC CTCAGGAAGC CACTCTACTG 480
CCCCCAGCAG CTCCAGCTGC TCCCTGCCAC CTTCACTCAC AGAGGTGGGG TGAGGAGGCG 540
TCTGCAGCTT CCCCTGGCAC CTGCTGGGAC CCTCCTGCCA GGCTGGACAT GTTAGCCCCT 600
CTCACTGGGC GGGTGCCTGG CTGCATGAGC ACTCTGCCCA GGGTTCCCTG CCCAGTGCGA 660
TGGCCTGGTG GCAGCAGGGA TGTGGCATTC CACCCTTGAG TCCCTGGCTC CTGCCTCTGC 720
AGTCCCATGT CTATACTGAC AGACAACACT GTCCCAGCGA GGGGCAAGAG AACAACTGGA 780
CGCCAGGGTG TCCTGAAATA CCACCACCCA GGCCGCTGCT GAAAGCTGTG CCCAGCAGGC 840
ACTGCAGATG GTTCTGGACA AAACTGAACC TCGTCCTGTC CCTTGGGTGG CTGGCTAGAA 900
TGCTGCTTCA GGGAGGGGGC GCAGCCCCTC CTGGCATGGA AGGGGCCTAT TCTGAGGTCC 960
CAGCATGGGG GCTCTGCATC CAGCCAGCAG CCTCACGGCA CCAGGTGACC CCAGGGTGGC 1020
TTCCCGCAGC ATGACCCCGA GGGCAGAGGG CCCACACCCC AGTCCCCATA GAACGAAACA 1080
ACGCTCCTCA GACCCACAGG CCCAGCGATT CGCCTCTCTG ACTCGCCCAG GACACCTCCT 1140
CCTCCCACTG CCACCTGGCC AGACCAACTC CCGGACGTCA GTGGCCAACA ACACCTCCAG 1200
CAGGAAGTCC CCCAGGCTCT GCAGATCCCA ACACTGACCA CACCAGGTCA ATGTGGCAAG 1260
ATGACCAGGG AGGTGGCTCT GAGACACCAG TTAGGATCCC CCAGAGGCCA CACAGCATGA 1320
GTCAGGCTAC CTAACCCCCT GAGCCTCAGT GTCCCTATCT GTCAAACAAA GACAGGAAGC 1380
AAGGCTGGGC CACCAGGAGA GGGCTGTGCT CAGAGGAACG CCTGCTGTGT GGAAGTGCTT 1440
CCGGAGGGGC CTAGTGCTCC TGCACCATTG CCTTGGCCTG CCTGGGGGCT CCCAGGAGGC 1500
AGGGACCGTC CGTACTGTGT CTGTCCCTGC CTGCTGCCAC TGTGGTCCCA GCACCTAGCC 1560
AGTAACCTCC CCAGGTTGGC CACCCCTCTT CTTCCTCCTT CTCCTCAGAG GAAAGCTCTA 1620
GCCTGGCCGT CCACCAGGAC CCACAGGCTC CTGGCGAGCC CTGCTCGCCA GGGCACACCT 1680
GGCCCTCTTT CCCAGGCAGC CAGCCCTCCT GGGACCCCAC CCAGCCCGGG AGCCGGATGC 1740
CAGGTCACGA GGGAAGCCTG GAAGATTTCT TGGAACACGG GATCCAACCG GCCCACAAGG 1800
TCACAGGGTC ACAACCAGAG CCTCAACAGG GCTCCTGCTC CCAGCCCTTC GGCCACACCC 1860
TGGGTCCAGC AGCCGCCCAG GGCTAGAGTG ACACAGGGGG CTCTCACGGG CCTGCACTGA 1920
GGTTCCCCAA ACGCAGAGCC CCTCTGGGCC CTGGGATATG ACATTGCATT TTGATCCTTG 1980
AAACCAAACT GTCATGTACC CTCAGGGACA GCTCAGAGGC AGGGACGGCC CAGGGGACCC 2040
AATGGGCACA GTGCCTCTGT CTGAAGCCCC CACCCTGGTA CCAGAGGGGC CACCCTCACT 2100
GTCATTCCCG ACTGGACTCA GGGCCCGGTG GCCACTTTTA GACACGGGTC TTCCCGGCTG 2160
TAGGACGGAC AGCCGGAATG CCACACACTG TTTCCACCCC CGCTCAACAC CGATCCCAAG 2220
GCGCTGGGTT CCCCAGGGCG CGGCGCGGGC 2250