EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-18492 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr19:13282810-13284510 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2AMA0052.3chr19:13283899-13283911TCTATTTTTAGT-6.27
MEF2BMA0660.1chr19:13283899-13283911TCTATTTTTAGT-6.32
MEF2CMA0497.1chr19:13283898-13283913TTCTATTTTTAGTAG-6.57
Nkx3-2MA0122.3chr19:13284463-13284476TTTAAGTGGTTGA-6.24
Nr2f6(var.2)MA0728.1chr19:13282819-13282834CGATCTCTTGACCTC-6
ZNF263MA0528.1chr19:13283477-13283498TCTCCTGCTTCCTCCTCCTCT-6.89
ZNF263MA0528.1chr19:13283474-13283495CCCTCTCCTGCTTCCTCCTCC-7.55
ZfxMA0146.2chr19:13282842-13282856CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 59             
IDCoordinateTissue/cell
SE_00539chr19:13282666-13283933Adipose_Nuclei
SE_00965chr19:13282922-13283865Adrenal_Gland
SE_01884chr19:13282779-13283855Aorta
SE_01884chr19:13283922-13284676Aorta
SE_02943chr19:13282817-13283735Bladder
SE_09569chr19:13282436-13284785CD14
SE_10284chr19:13282735-13283809CD19_Primary
SE_10284chr19:13283882-13284537CD19_Primary
SE_11152chr19:13260138-13284995CD20
SE_12008chr19:13282546-13284637CD3
SE_13717chr19:13282838-13283727CD34_Primary_RO01536
SE_14456chr19:13282559-13284868CD4_Memory_Primary_7pool
SE_15461chr19:13282687-13283828CD4_Memory_Primary_8pool
SE_15914chr19:13282532-13284498CD4_Naive_Primary_7pool
SE_16444chr19:13282666-13284044CD4_Naive_Primary_8pool
SE_16902chr19:13282758-13283877CD4p_CD225int_CD127p_Tmem
SE_17360chr19:13282708-13284917CD4p_CD25-_CD45RAp_Naive
SE_17844chr19:13282139-13284745CD4p_CD25-_CD45ROp_Memory
SE_20072chr19:13282719-13284828CD56
SE_20795chr19:13282835-13284138CD8_Memory_7pool
SE_21526chr19:13282726-13284048CD8_Naive_7pool
SE_22040chr19:13282555-13284797CD8_Naive_8pool
SE_22453chr19:13282550-13284786CD8_primiary
SE_23096chr19:13282822-13283769Colon_Crypt_1
SE_23766chr19:13282855-13283720Colon_Crypt_2
SE_24716chr19:13282813-13283841Colon_Crypt_3
SE_25952chr19:13282528-13283694Duodenum_Smooth_Muscle
SE_26584chr19:13282790-13283859Esophagus
SE_26584chr19:13283929-13284508Esophagus
SE_27635chr19:13282716-13283863Fetal_Intestine
SE_29636chr19:13282811-13283820Fetal_Muscle
SE_29636chr19:13283874-13284630Fetal_Muscle
SE_31408chr19:13282711-13283858Gastric
SE_34050chr19:13282766-13283818HCC1954
SE_34050chr19:13283927-13284422HCC1954
SE_34633chr19:13282456-13284846HeLa
SE_36380chr19:13282836-13283630HMEC
SE_37565chr19:13282583-13284411HSMMtube
SE_38051chr19:13282703-13283922HUVEC
SE_40852chr19:13282798-13283843Left_Ventricle
SE_40852chr19:13283901-13284570Left_Ventricle
SE_44417chr19:13282767-13283873NHDF-Ad
SE_44417chr19:13283891-13284592NHDF-Ad
SE_44845chr19:13282794-13283832NHLF
SE_47439chr19:13282531-13283956Panc1
SE_47495chr19:13282855-13283347Pancreas
SE_48836chr19:13282775-13283951Right_Atrium
SE_48836chr19:13283970-13284575Right_Atrium
SE_50086chr19:13282791-13283817Sigmoid_Colon
SE_52361chr19:13282734-13283815Small_Intestine
SE_52361chr19:13283915-13284496Small_Intestine
SE_53312chr19:13282707-13284541Spleen
SE_55159chr19:13282846-13283618Thymus
SE_56946chr19:13282855-13283489VACO_400
SE_57396chr19:13282819-13283326VACO_503
SE_57920chr19:13282985-13283402VACO_9m
SE_62354chr19:13259874-13293454Tonsil
SE_65341chr19:13282543-13283919Pancreatic_islets
SE_67827chr19:13282725-13284517u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191328289113283725
Number: 1             
IDChromosomeStartEnd
GH19I013160chr191327120013285018
Enhancer Sequence
GGATGGTCTC GATCTCTTGA CCTCTAGATC TGCCCGCCTC GGCCTCCAAA AGTGCTGGGA 60
TTACAGGCAT GAGCCACTGC GCCTGGCCAG GAGCATGTGT TTTCTCATCT TGGGCCTGGA 120
TCGAGTCCTT ATGGTGGAGG TGATCTGCGG GTTCCAGAAT CTTGGGAAGG GATTGGTGAG 180
ACCATAGCAT GGCCCATTGC ACCGTCCCTC TACCTGGAGT GAGGGGTGCC AGCCTCCCAT 240
TTCCTGGTGG GTGGGCTTGC TGGATGGCAG CCTGAGGTGG GTGGAGTCAG GCTGCCTTGT 300
TCTATTTCCT GGTTCCCAGG GTTGGGTGGT GGCAATGGTG GCCCCGGAGC CAGAGGGCTT 360
GGGGTACCCT GATCCTGCCT CCGGATTTAC TGGGTGGGTG CTAGGGTGTG TGCTCCAAGA 420
CCGATGGCCC CTGTGGGCGT GGAGGAGAAA CCAGAGACTC AAGCAGATCT CCCTGCCTGC 480
CTTCTGCCCT CATGTCCCAC TTCACCTTGG CTCTAGGCCA GGGGCTGCCA GAATGGTGAC 540
TCAGAGCGAC TGAGAAGAGG AGAGAAACAG AATGGAGGTC CTTATCATCC TCCAATCTCC 600
GCCATCCCAG CATCCCCATA AAGGTCAGGA CCCTTGAGGC CACATGTCAA GACCATCCAC 660
ACTGCCCTCT CCTGCTTCCT CCTCCTCTAC CCGCCCTCTT TCAGTGGGAT TTTTTTTTCC 720
GGGTACCACG CTAGGGCAGG AAGGCAGAAG TGAGCATGGG GCGTGGAACG TCTCTGAGGT 780
TGGAATATAT TTAGGCCAGG AGAAGAGTGT GTGTGTGGTG CTGGCCAGGC CCTGGCGCCG 840
GCTCGGCGGG CTTGAGGAGT GATGGTGGGG GGCCCTGAGC CAGTGTGGGG ATGCTCCTGC 900
CTTCTCCCTT TTTTTTTTTT TTTTTTTTTG GTTTTGAGAT GTAGTCTCGC TCTGTTGCCC 960
AGGCTGGAGT GCAGTGGTGC GGTCTTGGCT CACTGCAACC TCTGCCTCTT TGGTTCAAGT 1020
GATTCTCTTG CCTCAGCCTC TGGAGTAGCT GAGATTACAG GCATCTGCCA CCACGCCCGG 1080
CTAATTTTTT CTATTTTTAG TAGAGATGAG GTTTCACCAT GTTGGCCAGG CTGGTCTCCA 1140
ACTCCTGACC TCATGATCCG CCTGCCTCGG CCTCCCAAAG TGCTGCGATT ATAGGTGTGA 1200
GCCACCGTGC CTGGCCACCT TCTCCCTTTT AAAGACAGCC TGTCAGCTTT GGGGAGGAGG 1260
AGTGGGAATC ACTAGGCCCC CACCAAGGCT GAGGCAGGCC CTGTGTGGGC CAGATACATT 1320
TAGCATCTTC AAAACAAACC AGCAAGACTA ACATCAGGAT CACTTACAGC TGTAAACACA 1380
AGGCCCAGAG AGGTTAAGTG GCTTTCCCAA GGCTGTTCAG GAAAGAGGTG ATGATGGAAG 1440
GGTTCTCTTG CTGGCCCGGC TGGCTGCCAC CATTCATGCA CGCAGTGTTC ATTCATGCAA 1500
CACCTTTGTG GGTACAGCCT AGCCTGTGCC AGCCCCCAAC AACGTGCGGG AGAACAAGAA 1560
GCCAACTGGA CCCAGGTCGG CAAACCGCAG CCCATAGGTG GCATTCGTCT GTTGTCTCTG 1620
CACGGCCCTT GGGCTAAGAA TGGTTTTTAC ATTTTTAAGT GGTTGAAAAC AAAAGAATAA 1680
GAGTATTCCA TGATACATAA 1700