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

TagContent
EnhancerAtlas ID
HS116-12323 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr15:75076800-75078340 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1378942chr1575077367hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr15:75078172-75078190CCTGCCTTCCCTTCTCCC-6.39
NFIAMA0670.1chr15:75077775-75077785ACTTGGCACC-6.02
ZIC1MA0696.1chr15:75076958-75076972CACCGCAGGGGGGC-6.2
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_04703chr15:75074612-75078413Brain_Anterior_Caudate
SE_06487chr15:75074743-75086330Brain_Hippocampus_Middle
SE_09355chr15:75067239-75088089CD14
SE_10257chr15:75074656-75086515CD19_Primary
SE_11034chr15:75065304-75094638CD20
SE_11989chr15:75074828-75083464CD3
SE_13273chr15:75076998-75078513CD34_Primary_RO01480
SE_13668chr15:75074372-75086369CD34_Primary_RO01536
SE_14817chr15:75072034-75086364CD4_Memory_Primary_7pool
SE_15673chr15:75074377-75083288CD4_Memory_Primary_8pool
SE_16186chr15:75075959-75081759CD4_Naive_Primary_7pool
SE_16686chr15:75076419-75083026CD4_Naive_Primary_8pool
SE_16984chr15:75072134-75086617CD4p_CD225int_CD127p_Tmem
SE_17459chr15:75068139-75093490CD4p_CD25-_CD45RAp_Naive
SE_18711chr15:75067827-75089496CD4p_CD25-_Il17-_PMAstim_Th
SE_19500chr15:75072172-75083893CD4p_CD25-_Il17p_PMAstim_Th17
SE_20062chr15:75072048-75086531CD56
SE_21276chr15:75072313-75083423CD8_Memory_7pool
SE_21889chr15:75074448-75083401CD8_Naive_7pool
SE_22544chr15:75074693-75089542CD8_primiary
SE_26674chr15:75072103-75083500Esophagus
SE_31121chr15:75074653-75083398Fetal_Thymus
SE_32226chr15:75072112-75077290Gastric
SE_32226chr15:75077510-75083321Gastric
SE_32596chr15:75072108-75086152GM12878
SE_42830chr15:75074351-75083542Lung
SE_43649chr15:75065057-75083705MM1S
SE_49426chr15:75074355-75083350Right_Atrium
SE_50244chr15:75072089-75083506Sigmoid_Colon
SE_53145chr15:75074359-75083425Small_Intestine
SE_53381chr15:75072087-75083632Spleen
SE_55170chr15:75076769-75083359Thymus
SE_58450chr15:75053929-75093510Ly1
SE_58842chr15:75062849-75093607Ly3
SE_59668chr15:75063027-75093382Ly4
SE_60447chr15:75062747-75092923DHL6
SE_61139chr15:75063163-75092918HBL1
SE_62279chr15:75062911-75093525Tonsil
SE_66704chr15:75074888-75078330Jurkat
SE_67370chr15:75065057-75083705MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr157507710975078335
Enhancer Sequence
AGGGCCTTTG AAGAAAGGAG TCTGGCTTCT GGCTGGCACG TGTGCAGGGA TGTGCTTTTC 60
ATTGGTGAGC TTGGTGCCCT CCACCCTCTC AGAAGCAGCT GCTCTTCTCT CTGCATTGGG 120
TCAGGGGCAA GGAAAAAGCA GAAAATGTTC CCATTCACCA CCGCAGGGGG GCCAGACCCC 180
AAAAGGCTGA GCCACACAGA GTGGCCCTCG GCAAGGGTTG GAAATTTCGG GGACAGAATG 240
CAGCTTCCTC CAAACAAGTA TAGGTAGGGG TTGAGACCCA GGATCCACAG TGTGACATGG 300
CTGCCCCCCA AAGGGGGCAG ACCCACCTGG GTGCGGTTCT GGGCTCCATC TTTTGAAGGA 360
TTTTAAAACC TTGACAGGTC ATCTTCAAAG AGCCAGGGAT GTTGACTGAG TCTGGGAAAG 420
AGAAAGTAGG GACAGATTCT CATATGTCTG AGGGACTGTC CCAAATGAGA AAGGCATCCC 480
ATGGCAGAAA TTGTCCCAGA CACGTGGGCC AGAGCTAGGG AGCAGGTGGG TCCCAGGGAA 540
GTGAATCTGA GCTCATTATA GGGAAACCAT GAATGTACTC ATTTTCTTGA TTTAGAAAAT 600
AACAAAACAG CGCTACAGGA AATTTAGAAA ATGAAACAAA AATCACCCAC TATTTCTTCA 660
GCAGGCAGTG ACTGTGTTAG CATTTTGGAG TTCACTGCCA GTCTTTTCCC CATCCTTTTC 720
CTTCATTGTC GTTGTCACTG GAGTGTGTGT GCCGTGACAC CTTTTTTCAT TTAATACTGC 780
GTCTGTGGGC ATTTTCTCAT GGTGCTACGC GGTCTAAGTA ACGTTGCTTC TAAAAAGCTA 840
CAGAACATTC TAGGCTGGCC TGCTGCAGCG CCATCACCCA TACACTGGAG CGTGTGCATT 900
TTTCCCCTCT GTTGCTGTTG TGGTTGTCGT TACTATGAGT CCCAAAAGCA GCCAGGGTGT 960
TGGAGGGCAC AAGCAACTTG GCACCCAACT GAATGTGGGT TCCAGGCCCA GACATGCCAC 1020
TTAGGCCCAG GGTAGAGGGA CCTTAGACAG GTCACTGACC TGCTGAGCCT CGTTGATATA 1080
AATAACAGGA TGGTAACACC TACTTCAGAG GAAGGTGTAA GGACAGTGTC AACTAACTAA 1140
CCAAGGGACT CTAAAGTGCC TGGCACAGCC CTTTCTTCAC TCCCTCTGTG AGTAGGATTG 1200
GCATTGTTGA AGGAGTGCCC ACTGCTGGCT GCCTCAACCT GTGGGGAAGG TGCCTGAGCC 1260
ACGGGCCAAT GTTGACTGAC CACTCACCTG GCAAAGAGGT GGTCTCCGCC TGAGGAGCCC 1320
CTGTGAAACC CCCTGGCCCT GAGGTTCTAG AATACTATGG CCAGTGCCCT TGCCTGCCTT 1380
CCCTTCTCCC CATTACCATA TGATTGGCTG GCCTAGGACA TGGGGCTGGC CCTGGGAAGA 1440
TGGGCTGCTG GTTAGGGTCC GGGACCTGAC TCCACCCATT CCCCTTCCGG TCTCCCAGCA 1500
TCAGAGCTAA ATAGACAAGG CCTCTTCTCT CTCTCTCTCT 1540