EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS042-19245 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr17:37029890-37032470 
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
ATGGGGGCGT GGGGCCACTG GGAATAATCC TGTCCTCCTC GGAATTTGTG GAGGTGCAGC 60
AAAGATCTAT GCCTTTAAGC CAGCGGGTCA GGTGGCCAAC CAAGCTAGGC TGGTGCCCCG 120
GCCAGGGTGG GGCTGGCATT GCCTCTGCAG GAGGGAGAAA CTGTAACCCT GGGCAACAGG 180
AAGGGAAGAG ATGGTCTCAT AATCCATCCC TGAGTCATGG CCACCCCAGG TAGCCTGGGT 240
TCAGAGGCCA AGGTGCCAGG CTGCAGGCAC AGTGACACGA AGCTTGCCAC ATCCCCCCCA 300
ACCCAGAGCC ACAGAGGGAC AGGCTGTCCC AAGTGAGGGG TATCCTTGCA GGCTTCTGCC 360
CCTACCAGCC TGTTTACCTT TCTTTAGAGT GGGTTGCAGG TAGGCAAGGG AAGATCAAGA 420
TGACCCTGCC TTGGAGCCTC GGATCCAGGC TGAGAGGCCT CTAACAGGCA GCAGAGGTAG 480
GGTCTGTCTG GTTTCTGTGA ACAGGGAAGC CATGGACTTT GCAGGCAGCA GGAAGGGGCA 540
GAGGTGCATG CCTCGAGGTG CAGTTTCCTT GAGTCCTGAG GCCCAGGAAT GCTTCGCTGA 600
AATCATCTTG CCTGGGGCCT TTAAAAGAGG GGGGCTCTTG CTCTGGGACA GAGCCCATGG 660
GGCAGGGCAG AGGCAGACGG GGTCACTGTG GGGTCCTCTG GACATATTTC CCTGACAGTG 720
TCCTTCCCCA GACCCCATTG AGACAAGGCA GGAGTTCTTT CATCTTAGGG TCCAGGCTTG 780
GCTCACAGCG GTTGTGGAGG GACTGGCCAT TTTCTGCCTC CCCTCCCCAC AATTTTCCTA 840
CCCCAAAAAG GACACAGTGG AAGGAGCTGG TGGGTTTTCT TGAACCTTGG GGCCTTCCTC 900
CAGAGAGGGT AGGGGAGTCG CCTGAAGCTG CTGGAGGTGC CAAGCATTAG GGGTGGAACG 960
GCCTCCTCTC CTGACCTTCC AGCACTCTGG GAGACAGTGG CTGCAGCTCC ACTTGACACT 1020
TGTGCTTCAT AGTAACTGGT TTCCATGTTT CTGCTCAGAG CCCCCTGCAG GGGGACAGGC 1080
GACCACCCTC CTCTGCCCCA CCCTTGGGTG TCTGGATGAG AGTGTGGGGC CTGTGAGGGA 1140
GGTGGGAAGG AGCTACTGAT AGAAATAGGT GCCATCCCCT AGAAGAGGGG CTCTGCTTCC 1200
TCCGCGTGGC AGCCTGGAGG GGTCTTTGGA ACCACTGGGT CCAGTGTTGG CCCTGTGCCC 1260
CCTGCCTGCT CAGTACACCC CACCCTCCTT CTCCAAGGGG CTTGGCTCCG GGTGCAGGCC 1320
TGGCCATCTG GAGTAGGGGT CTCTCTCCCT TTGTCTCCCC AACGTCAATC AGGAGGCAGC 1380
CTTGGAGGTC CGTGGTCCTA GGACAGTGTG TAGCCCTTCG TGTGTGTGTG TGTGTGTGTG 1440
TGTGTGTGTG TGAGAAAGTG GGTCATGGTC TGGATTCTGG AGAATGTTTT TCCTGGCAGG 1500
CCCCTGTGGG GGTAGGGGGA GGCAGGGGCC CAGGCAGGGG CCTAGGCAGG GGCCTGTGCA 1560
GCTAAGTAGG CAGAGGCCAG CAGACTGGGT GGTGACCAGG CTGGGGCACC CTGCCAATGC 1620
CTCCCAGTTA CTCGGGGAGG GAGTGGGGCT GTCACTTCAG GGGCCTGTGG GGGCAGGGAC 1680
CAGCCTGTCT TAGTGTCCCT GGTGGGTTCT GTGTGTTGGG GTATGCACCA CTTCAGGGGC 1740
CTGTGGGGGC AGGGACCAGT CTGTCTTAGT GTCCCGGTGG GTTCTGTCTA TTGGGTTATG 1800
CACCAGAAGG AGTCTTTAAG TTGCCTCATA GGAGTTTGGG GGCCCTGGGT CACTGGGATA 1860
GGCCCAGGTT GGGGAGGGGG CCAAGCTTAG ACCCGCCACT TCTTTGCTTC CAGACTTCCG 1920
GCTGGCCGTC CTCCCCAAGA GTGGTTCTCC TAGCATTCTG TTTAATATTC CACCATTAGG 1980
TTTTTCCTTT GGGTCTTCTT GATAGGGAAC CAGTACCCTA TTAGAAGGTG ATTTCCCCCT 2040
GAAATTACCC TGGGGGTCTC TGGTTGAAGT GGGCCATGGT AGGGAGGTTG AATCCCAGAT 2100
TCTCAGCCTT CTTTCTGCTA TCCCCTCCTC CCAGTGTCTC AGAAGCACCT CTCCCTCCGG 2160
GGGTTTGGAG ACAACATTTT GAAAAGCATC GCCTTGGGGG AATTCCTTGA CAAATGGCCA 2220
AGAACCAGCT CTGTGGCTGG GCTCCTTCAA AAGTCCCCCT GGGCCTGCCT CCTGGCCTCC 2280
TTCTTTTGGA ATGGGGAATG TCTCCCTTGA CTACTGGGAA ATGGGGCAGG GACAGGCCAG 2340
CCAGGTCACT CAGGTGGCCT GGATTATTCT GGGGTCCTGG CAGTGGACCC CTGTTTGGTG 2400
GTGATCCAGC ACATCATCCT GGGCTTCTGG GGGTGAATTT AGATCCTGTT GTCATGGGTT 2460
TGCCTAAGCA TCAATACTTC TCAGGGGTTC CACAAAGACC CCTCCAGGCT GCCACGTGGA 2520
GCCTGTTAGA TCGTTTCTCT TTTTTTTTTT TTTTTTTTTG AGACAGAGTC TTGCTCTGTC 2580