EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-11606 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr15:67467050-67469690 
SNPs
Number: 5             
IDChromosomePositionGenome Version
rs12912010chr1567467143hg19
rs12912045chr1567467297hg19
rs12913547chr1567467507hg19
rs17294280chr1567468285hg19
rs35251008chr1567468525hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr15:67469246-67469256GGCACGTGCC+6.02
HES2MA0616.2chr15:67469246-67469256GGCACGTGCC-6.02
RELAMA0107.1chr15:67467407-67467417GGGAATTTCC+6.02
TBX21MA0690.1chr15:67467969-67467979AAGGTGTGAA+6.02
TBX2MA0688.1chr15:67467969-67467980AAGGTGTGAAT+6.02
ZNF263MA0528.1chr15:67467455-67467476GAAGGAGGAGGCAGGTGGAGA+6.44
ZNF263MA0528.1chr15:67467458-67467479GGAGGAGGCAGGTGGAGAGAG+6.66
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_09181chr15:67466836-67470715CD14
SE_10875chr15:67463174-67471168CD20
SE_18371chr15:67463340-67469893CD4p_CD25-_Il17-_PMAstim_Th
SE_23212chr15:67466304-67468217Colon_Crypt_1
SE_26536chr15:67466309-67469672Esophagus
SE_31411chr15:67466416-67469347Gastric
SE_37787chr15:67466568-67472740HSMMtube
SE_37941chr15:67465373-67472958HUVEC
SE_38928chr15:67462159-67469899IMR90
SE_42172chr15:67467092-67469654Lung
SE_44471chr15:67467419-67472425NHDF-Ad
SE_44749chr15:67466055-67469674NHLF
SE_45534chr15:67453126-67473814Osteoblasts
SE_47100chr15:67357928-67475420Panc1
SE_48052chr15:67464183-67473310Psoas_Muscle
SE_50064chr15:67466721-67469446Sigmoid_Colon
SE_51081chr15:67466500-67469701Skeletal_Muscle
SE_51874chr15:67467444-67469444Skeletal_Muscle_Myoblast
SE_52344chr15:67466124-67469783Small_Intestine
SE_63662chr15:67467303-67469755HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr156746817167468380
Number: 1             
IDChromosomeStartEnd
GH15I067171chr156746362167474069
Enhancer Sequence
GGGAGCTCTT CCTAGGAAAA AATGGGGACA TCTCAGGACA TCTGATTATT TCCTTTAAAG 60
AGATTATTAT GAAATTACTG TACAAAAAGA AAGAAAGCAG AGGACATCTG GTTTCTCCTT 120
TCATTTCCTC CCCACTCCAG GTGTTAGCCC CAGGGCTCAG GTCTGGGGAA GGTTGAGCCT 180
CCTTGCCCCA GCAAAGCCAC TTCTGGTAAG GGGCAGGGAC TCCTGGTTGA GACCTGGCTC 240
AGCATCCTGC CCCAGGCAGG CTCTCGGAGA CCCTGGGACC TGGGACCGTT GTTTGCAGGG 300
CAGGAGATAT GAGCAGGTGA TGTTCCTGTT ATTACACAGC GTGCTGGGTG AGTCACCGGG 360
AATTTCCTAG GCATTTAAGG CGGAAGGATT GGGGTAAATG GAGGGGAAGG AGGAGGCAGG 420
TGGAGAGAGG AAAAAGGTAG TGAGCTGGCT TCTGCCTGGT GAGTAAGTTG TTCCCTGCTT 480
TAAAGTGAGA TGATTAGGGC GGAGCCATGA CTGAGGAAAA TAATGTACCA GGGAGAGCCC 540
TGAGGGAGCA GTTGAGCTGG AGTTAAAGGA GGTGATGGCT TCCAGAGTGC CAGTGGCAGG 600
AGTGAGAGGC AGGGATGGGG CAGCTTGGAG TGAGAGGGAT AGGGCAGCTT GGAGGTGGCT 660
GATGCCGGAT GCAGTGCTTC AGACTGAAAG GTGGTCGTTT GCTGTGAATT GCCCTCTAGA 720
TTGTGTAGAC TAGGATGATG GGATGTTTCT TGAGCTTGGA CCCAAGGCAG CATCTCCTGT 780
TGACATAGTT CTCCCTCCCT ACTGACGCTT CCTCAGGCAC CTTGCCTGAG AGTTGAGAAT 840
TCTTAGGTTA TTTCTTCCAA AGGGAGGACC CTCCCCCCAG GGTGCCACTT TGCACTGGCC 900
TAGTTGCACC TCTGCTGGGA AGGTGTGAAT CGGGGGCAAG TTGCCCCGTG AGTCAGGGTT 960
AGGATTCTGG GTGAGACTCC ACGCTGACAG GCCCGGCTTC CCCTCTGCTT CATGAGCCCC 1020
TGTGCCCATG TGTGAGCACA GGTGTGGTGG CAGGGCGGCC CGAAGACCAC CAGCCCTGAG 1080
TGTGGACGGC GGCCCAGGGC AGAGGCCCAA CCCAGTTCCA GGCATCTTCA TGCTGCTGCC 1140
CAAGGCTCTT TTACAATGCA GCCTCTGGCT CCGGTCTTCC CCACACTTGT GAAATCACAG 1200
GCAGGGTCTT CCCCACACTT GTGAAATCAC AGGCAGGCAA CATAATGACA GGAAGTCAGC 1260
TGTCGGCTCT GTCTTCATAC TCCTGAGGGC CCGGTTTTTA GACTTTGCCA CTGTTCCTGG 1320
TTGCAGTATG CTGGTCATAA GCTAAAAGGG CATGGGGGTC TCTGTGCAGC TTGGTTTGGT 1380
ATTTTAGTCC GCAGATACAT AGGTTGGAAT TAGTACCCTG GGTGCTGGGA CACAGCTGGC 1440
GTGGGCTCAC AGAGACCTCA TCCTCTAGCA TAGGAGACTC AGGTACACAG TTTCTGGGAC 1500
ACAAGGTTAA TTCTGCACTG AGGCAGTGAG GGAGTGTTTC ACAGCCGTGT GAGCTGGGCC 1560
TTAAAGATCG AGTCCCTGCA GAGGAGGGGG ATGGGCAGTC CAGGCAGAGG ACCCAGGCAG 1620
GACTGAGAAG TGGTGGATGA GGAACATGGG AACTGGAGTG TGGAATCTCC TAGATTGAGG 1680
AAGAGCTGCC TTCCGCAGGT GAGGTGGGCC CAGCAGAAAC CAGCCCATTT CTGTTTTGAC 1740
CTTTCGTCTT GCAGCAGCAG TGCTCCTGGC CTTTGCCCGT TCCTTGCTTT CGATTTATAG 1800
GAGAAAGTTA ATTTCCCCCC TTGCCTCCCC ACCTCTTCCT TTACGGGATT TGAATCTCTT 1860
GCACATGTTT TTAATAGGCA TCCCTTAATC CAAGTGTTGC CTTCTGGGTT TTATTCTGTT 1920
TTCTTTTTCT TAAACATAAT GGAACGTCTG TGCCAGCTTG GAACAGGACT GAAAACTGAG 1980
GCCAGCCAAT GCGTTAGGCT GGCAGGGGGC CAGCCATGGA TTAAGTGCCC TATGGCACTT 2040
GAGAAGTCTG GCCGACACCA CACTGGTGGG GGAGGGGGAT CCACAAAGGC TGGAGCTGGA 2100
GGTTCCTGCG TCTCCAACAC CTCTGCACTG GGAGGAGAGA TTAGCACAGA CTCAGAAATC 2160
TGGCCAGGAG CAGGGCTGTT TGAAGGGAAG GCCGTGGGCA CGTGCCATCG TCTACCACCC 2220
CAGCTGTGCA AAATGCTCAG CCTAGAGGTG AAACTGCTCT TCAATGGGGT GTGTCACCTT 2280
ACCCCCCGTA GTCATTCTCC TAGAGGAGCC TTCTATAGAA CTGCTTCTGC ATTTGTTGGT 2340
AAATCCTTGA AACCAGATCT TAATTTGCTT GCTTGCTTGA TCAGTTGATT GATTGGTCAG 2400
GGGAGGGGTT GCCACCTCCC CCTGAGAGAT TTCTTTTAAG ATTTAATGCC AGGACAAACT 2460
TTGTTTTCCC TGAGGAACTA GTAAGCATTG CCCATCCACC AACCAGAGCC ATAGACCATG 2520
TCATGTTCCC TTTTTGTCTT GTCTACTAGG AAGCTCAGAG CCAAACTGGA TGCTTTTGCA 2580
GTAACTATAA CCTCATGGTT ATCCCATTTA TAGCCGCCTT CTTTCCAGAG TCCTTTTTGT 2640