EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS191-16098 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr17:37029840-37032410 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs140564516chr1737029972hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr17:37030300-37030317AAGATCAAGATGACCCT+6.05
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_01190chr17:37029988-37031536Adrenal_Gland
SE_01190chr17:37031562-37032414Adrenal_Gland
SE_01869chr17:37023855-37032525Aorta
SE_04550chr17:37029789-37032228Brain_Anterior_Caudate
SE_06121chr17:37023495-37032660Brain_Hippocampus_Middle
SE_08151chr17:37023817-37032421Brain_Inferior_Temporal_Lobe
SE_12286chr17:37030121-37030837CD3
SE_19419chr17:37029749-37030890CD4p_CD25-_Il17p_PMAstim_Th17
SE_19419chr17:37031063-37032540CD4p_CD25-_Il17p_PMAstim_Th17
SE_20407chr17:37023792-37032439CD56
SE_22571chr17:37024177-37032603CD8_primiary
SE_23506chr17:37024967-37031810Colon_Crypt_1
SE_24046chr17:37029821-37031666Colon_Crypt_2
SE_26978chr17:37023774-37030539Esophagus
SE_26978chr17:37030815-37031917Esophagus
SE_27795chr17:37023628-37032219Fetal_Intestine
SE_28678chr17:37023614-37032233Fetal_Intestine_Large
SE_31106chr17:37023889-37032555Fetal_Thymus
SE_31542chr17:37023821-37032501Gastric
SE_42353chr17:37023756-37032469Lung
SE_47849chr17:37030061-37030517Pancreas
SE_48905chr17:37023784-37032426Right_Atrium
SE_50172chr17:37023747-37032545Sigmoid_Colon
SE_52400chr17:37023741-37032508Small_Intestine
SE_53492chr17:37030086-37032145Spleen
SE_55164chr17:37031219-37031860Thymus
SE_59348chr17:37019329-37056453Ly3
SE_62887chr17:37023359-37058235Tonsil
SE_65628chr17:37024882-37032382Pancreatic_islets
SE_68729chr17:37029305-37032442H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr173702991937030193
chr173703108737032408
chr173703080837030985
Enhancer Sequence
CATCCCTTCC TGACCCTATC TGGAGGAATG CTCTGGGCCT GGGGTCTTGT ATGGGGGCGT 60
GGGGCCACTG GGAATAATCC TGTCCTCCTC GGAATTTGTG GAGGTGCAGC AAAGATCTAT 120
GCCTTTAAGC CAGCGGGTCA GGTGGCCAAC CAAGCTAGGC TGGTGCCCCG GCCAGGGTGG 180
GGCTGGCATT GCCTCTGCAG GAGGGAGAAA CTGTAACCCT GGGCAACAGG AAGGGAAGAG 240
ATGGTCTCAT AATCCATCCC TGAGTCATGG CCACCCCAGG TAGCCTGGGT TCAGAGGCCA 300
AGGTGCCAGG CTGCAGGCAC AGTGACACGA AGCTTGCCAC ATCCCCCCCA ACCCAGAGCC 360
ACAGAGGGAC AGGCTGTCCC AAGTGAGGGG TATCCTTGCA GGCTTCTGCC CCTACCAGCC 420
TGTTTACCTT TCTTTAGAGT GGGTTGCAGG TAGGCAAGGG AAGATCAAGA TGACCCTGCC 480
TTGGAGCCTC GGATCCAGGC TGAGAGGCCT CTAACAGGCA GCAGAGGTAG GGTCTGTCTG 540
GTTTCTGTGA ACAGGGAAGC CATGGACTTT GCAGGCAGCA GGAAGGGGCA GAGGTGCATG 600
CCTCGAGGTG CAGTTTCCTT GAGTCCTGAG GCCCAGGAAT GCTTCGCTGA AATCATCTTG 660
CCTGGGGCCT TTAAAAGAGG GGGGCTCTTG CTCTGGGACA GAGCCCATGG GGCAGGGCAG 720
AGGCAGACGG GGTCACTGTG GGGTCCTCTG GACATATTTC CCTGACAGTG TCCTTCCCCA 780
GACCCCATTG AGACAAGGCA GGAGTTCTTT CATCTTAGGG TCCAGGCTTG GCTCACAGCG 840
GTTGTGGAGG GACTGGCCAT TTTCTGCCTC CCCTCCCCAC AATTTTCCTA CCCCAAAAAG 900
GACACAGTGG AAGGAGCTGG TGGGTTTTCT TGAACCTTGG GGCCTTCCTC CAGAGAGGGT 960
AGGGGAGTCG CCTGAAGCTG CTGGAGGTGC CAAGCATTAG GGGTGGAACG GCCTCCTCTC 1020
CTGACCTTCC AGCACTCTGG GAGACAGTGG CTGCAGCTCC ACTTGACACT TGTGCTTCAT 1080
AGTAACTGGT TTCCATGTTT CTGCTCAGAG CCCCCTGCAG GGGGACAGGC GACCACCCTC 1140
CTCTGCCCCA CCCTTGGGTG TCTGGATGAG AGTGTGGGGC CTGTGAGGGA GGTGGGAAGG 1200
AGCTACTGAT AGAAATAGGT GCCATCCCCT AGAAGAGGGG CTCTGCTTCC TCCGCGTGGC 1260
AGCCTGGAGG GGTCTTTGGA ACCACTGGGT CCAGTGTTGG CCCTGTGCCC CCTGCCTGCT 1320
CAGTACACCC CACCCTCCTT CTCCAAGGGG CTTGGCTCCG GGTGCAGGCC TGGCCATCTG 1380
GAGTAGGGGT CTCTCTCCCT TTGTCTCCCC AACGTCAATC AGGAGGCAGC CTTGGAGGTC 1440
CGTGGTCCTA GGACAGTGTG TAGCCCTTCG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 1500
TGAGAAAGTG GGTCATGGTC TGGATTCTGG AGAATGTTTT TCCTGGCAGG CCCCTGTGGG 1560
GGTAGGGGGA GGCAGGGGCC CAGGCAGGGG CCTAGGCAGG GGCCTGTGCA GCTAAGTAGG 1620
CAGAGGCCAG CAGACTGGGT GGTGACCAGG CTGGGGCACC CTGCCAATGC CTCCCAGTTA 1680
CTCGGGGAGG GAGTGGGGCT GTCACTTCAG GGGCCTGTGG GGGCAGGGAC CAGCCTGTCT 1740
TAGTGTCCCT GGTGGGTTCT GTGTGTTGGG GTATGCACCA CTTCAGGGGC CTGTGGGGGC 1800
AGGGACCAGT CTGTCTTAGT GTCCCGGTGG GTTCTGTCTA TTGGGTTATG CACCAGAAGG 1860
AGTCTTTAAG TTGCCTCATA GGAGTTTGGG GGCCCTGGGT CACTGGGATA GGCCCAGGTT 1920
GGGGAGGGGG CCAAGCTTAG ACCCGCCACT TCTTTGCTTC CAGACTTCCG GCTGGCCGTC 1980
CTCCCCAAGA GTGGTTCTCC TAGCATTCTG TTTAATATTC CACCATTAGG TTTTTCCTTT 2040
GGGTCTTCTT GATAGGGAAC CAGTACCCTA TTAGAAGGTG ATTTCCCCCT GAAATTACCC 2100
TGGGGGTCTC TGGTTGAAGT GGGCCATGGT AGGGAGGTTG AATCCCAGAT TCTCAGCCTT 2160
CTTTCTGCTA TCCCCTCCTC CCAGTGTCTC AGAAGCACCT CTCCCTCCGG GGGTTTGGAG 2220
ACAACATTTT GAAAAGCATC GCCTTGGGGG AATTCCTTGA CAAATGGCCA AGAACCAGCT 2280
CTGTGGCTGG GCTCCTTCAA AAGTCCCCCT GGGCCTGCCT CCTGGCCTCC TTCTTTTGGA 2340
ATGGGGAATG TCTCCCTTGA CTACTGGGAA ATGGGGCAGG GACAGGCCAG CCAGGTCACT 2400
CAGGTGGCCT GGATTATTCT GGGGTCCTGG CAGTGGACCC CTGTTTGGTG GTGATCCAGC 2460
ACATCATCCT GGGCTTCTGG GGGTGAATTT AGATCCTGTT GTCATGGGTT TGCCTAAGCA 2520
TCAATACTTC TCAGGGGTTC CACAAAGACC CCTCCAGGCT GCCACGTGGA 2570