EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS155-07329 
Organism
Homo sapiens 
Tissue/cell
Ovary 
Coordinate
chr19:41830820-41832610 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12980942chr1941832231hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:41831463-41831481CCCTCCCTCCCTCCCTCC-6.03
ZNF263MA0528.1chr19:41831425-41831446CTCCCCTCTCTCTCCTCCCTT-6.48
ZNF263MA0528.1chr19:41831472-41831493CCTCCCTCCCTCTCCTCCCCA-7.29
ZNF263MA0528.1chr19:41831459-41831480CTCTCCCTCCCTCCCTCCCTC-7.43
ZNF263MA0528.1chr19:41831469-41831490CTCCCTCCCTCCCTCTCCTCC-7.46
ZNF263MA0528.1chr19:41831463-41831484CCCTCCCTCCCTCCCTCCCTC-7.97
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_01266chr19:41827473-41832460Adrenal_Gland
SE_01941chr19:41826114-41834937Aorta
SE_02341chr19:41827299-41835217Astrocytes
SE_06609chr19:41827940-41835020Brain_Hippocampus_Middle
SE_10534chr19:41829088-41835289CD19_Primary
SE_10928chr19:41826548-41839191CD20
SE_13335chr19:41827590-41831869CD34_Primary_RO01536
SE_14717chr19:41828274-41835424CD4_Memory_Primary_7pool
SE_17526chr19:41828356-41835571CD4p_CD25-_CD45RAp_Naive
SE_18470chr19:41828743-41831400CD4p_CD25-_Il17-_PMAstim_Th
SE_18470chr19:41831462-41835430CD4p_CD25-_Il17-_PMAstim_Th
SE_19170chr19:41828918-41831224CD4p_CD25-_Il17p_PMAstim_Th17
SE_19170chr19:41831258-41835426CD4p_CD25-_Il17p_PMAstim_Th17
SE_20013chr19:41827344-41835576CD56
SE_20919chr19:41828272-41831918CD8_Memory_7pool
SE_20919chr19:41832350-41835435CD8_Memory_7pool
SE_22408chr19:41828648-41835382CD8_primiary
SE_26210chr19:41827478-41831409Duodenum_Smooth_Muscle
SE_27131chr19:41827046-41832712Esophagus
SE_29782chr19:41829706-41832567Fetal_Muscle
SE_31885chr19:41826804-41832672Gastric
SE_37091chr19:41826651-41835398HSMMtube
SE_38093chr19:41826925-41835502HUVEC
SE_40475chr19:41828286-41832867K562
SE_41125chr19:41824878-41835177Left_Ventricle
SE_44313chr19:41826974-41833634NHDF-Ad
SE_44950chr19:41827136-41832669NHLF
SE_45824chr19:41826675-41835471Osteoblasts
SE_48776chr19:41825187-41832669Right_Atrium
SE_50262chr19:41826769-41835431Sigmoid_Colon
SE_52575chr19:41827074-41832699Small_Intestine
SE_54849chr19:41827115-41832913Stomach_Smooth_Muscle
SE_62666chr19:41801738-41841748Tonsil
SE_65513chr19:41830762-41832771Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194183164341832527
Number: 1             
IDChromosomeStartEnd
GH19I041321chr194182700941835422
Enhancer Sequence
ATGAGAGACA CAGAAATTGA GTCAGAATTA GGGTTAGTCA GATGGTCAAG ACGTGAGCAT 60
CTAGCTGACA GACAGAGGTG GAGCCAGTCC CAGGGACAGG GATTAGATGG GGAGACAGGA 120
AGAGAGGTGG AGACAGAGTG GGGTAGGGAT GACGGGAGAC ACACCCCCTG GTCACTGCCT 180
CTGAGACCTG GGGGTGGTGG GCCCCAGGGC GGGTGCCTCC CATCCCCCTC CCAGTTCTCC 240
CGGGGTCGGG GTAGGTGGAA AGGCTGAGTC AGGGAGGGCG GGCCCCGCTG GGAGACAACC 300
CCTAGGTGGG CATCCGGCCC CCACCCCCGT GTCTCCTGTC CGTCCTGGCC CTGGCCTGGC 360
TCGCTGGCCT GGCCGCCACC CCGCCCCCCA CGTCTGACAC CTCCATGCGT CCTGCCAAAG 420
CAAGCTGCCT CCCTGCACTC TTCCCCCTCC AGCTCCAGTC ACTCTGTCCC TCTGTCCCCC 480
GTCCCTTCTC CCTGCTTCTG TGCGTTTCTT TCCAGCCCTC TGCCTTCCTC CCTCACCGCC 540
ACTGCTCTGT CTTCTCGTTC TGTCTCCACA CCTCTGGCTG TCGGTGTCTC CCCGTGACTT 600
TCCGTCTCCC CTCTCTCTCC TCCCTTGTTT TTCCCATGCC TCTCCCTCCC TCCCTCCCTC 660
CCTCTCCTCC CCACCTTTTC CACTCCGTGT CCCCAGCCAT TCTCCATCTC TGTTCTCAGC 720
TCCTGTCACC TCGTTTCCCC ATCCCTTTCT CTGCTGGAGT CTCCCTCTGG GGGGCTCTGT 780
CCTCTCCTCA CTTTGCCCTT TCCCTCTCGC TGCTGTGTGT CTTGGCCCGC CCCCCGTGCC 840
CCCCATCTCC TCTGTCTCCC ACACTCTGGG AAGCCCGGCT GGGATATCCA GGTTGGAGCC 900
TCACTGGCGG CCACTGGAAA CCCAGAATGA GGGGTCATCG CCTCTCGCCC ACCCAGAAAG 960
GGCGCAGGAG GGGGCAGCAA GGTTGCGGGG CCTGTCTGGC CAGAAGGAAA TGTCTGTGCT 1020
GTGGCCTGGT CACCCCCGCC CCCAGGACCT GCTGGGCTGC TGCCGCCCCC GGCCGGGGCT 1080
GAGGCCGAGT AAACACAGCA AACACAGCCG CCGGCAGCCT GGGATATTTA TACCGAGGCT 1140
GGGCGTGGGT CCAGTGCCCA CCACAGCCCC TGCCCTGCCC TGCCTTGCCT GCTGCCACAG 1200
CCAGCTCCGA GCCAGCGTGG CACCAGCCGG CAAGGGGACG CGCCGCAGAC ACAGCCTGCG 1260
CTGGGTATGG AGGCCAACAG GCACTGGCCG CTCATGATGC AGGCGGCTCC ATGGACGCAC 1320
CCTGTCCCCC TCCCCTGAAA ACACCAGCAC ACAATGTGGA CCCACACTCG CAGCTGCTCA 1380
CAAACACACA TCCACCCCTG CTGAGAACGC GAAATCCCCT CAACGATGAT GCAAAACAGA 1440
CCCACACAAC TCCACACACT GCAGTCACCA GCCTACATGT GGGAACACAG CATGCAGACA 1500
CCACCTTAGC ACCTGCTCAC AGCACCCACA GGCTGGGAAC ACCAGTCCCT GAGATGGACA 1560
CACAGCCCCG AAGTACAGCC CTCCCTCACA CAGACAAACA CTGAGAACCA CAGGAAGCAT 1620
GCTGGATGCA CACCACGTAG ACAAACATGC TCAGAATACC AGCGACACAT GCACTGATCA 1680
CAGTGCAACC CAGAAACAAC TCAACTCATC TGCCTCATAT GTAAGAAACA CACACGGCCG 1740
GGCGCGGTGG CTCATGCCTG TGTCTCAGCA CTTTGGGAGA CCAAGGTGGG 1790