EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS060-19154 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr2:47229600-47232890 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17540621chr247229839hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr2:47231406-47231420GTGAGTCACTTCCT-6.15
RFX1MA0509.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.94
RFX1MA0509.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.95
RFX2MA0600.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.77
RFX2MA0600.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.83
RFX5MA0510.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.14
RFX5MA0510.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.27
RORA(var.2)MA0072.1chr2:47230175-47230189CTGACCTAATTAAC-6.05
ZNF263MA0528.1chr2:47231802-47231823GAATGAGCAGGAGAAGGGAGG+6.27
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_00056chr2:47228729-47233257Adipose_Nuclei
SE_00864chr2:47228939-47232656Adrenal_Gland
SE_01547chr2:47229049-47237427Aorta
SE_03148chr2:47228934-47232779Brain_Angular_Gyrus
SE_03864chr2:47224295-47237133Brain_Anterior_Caudate
SE_04790chr2:47207331-47238050Brain_Cingulate_Gyrus
SE_05773chr2:47203345-47237435Brain_Hippocampus_Middle
SE_06717chr2:47224482-47237491Brain_Hippocampus_Middle_150
SE_07731chr2:47224149-47237360Brain_Inferior_Temporal_Lobe
SE_08824chr2:47229662-47231117Brain_Mid_Frontal_Lobe
SE_08824chr2:47231233-47231571Brain_Mid_Frontal_Lobe
SE_09141chr2:47226225-47233894CD14
SE_26122chr2:47229467-47230939Duodenum_Smooth_Muscle
SE_26616chr2:47229058-47231804Esophagus
SE_26616chr2:47231831-47232707Esophagus
SE_48626chr2:47229031-47231103Right_Atrium
SE_53323chr2:47229516-47230518Spleen
SE_54495chr2:47226285-47245145Stomach_Smooth_Muscle
SE_65882chr2:47229163-47232588Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr24723098247231623
Number: 2             
IDChromosomeStartEnd
GH02I047001chr24722903247231739
GH02I047004chr24723183247232707
Enhancer Sequence
AAAGCAGGAT TCTGAGGCCA CTTCAATGGT GGAAGGGAAA GAGTGTGGCT GGGACTAGGT 60
CAGAGCTACT CCCAGAGCAT GGGGGTACAC CATGTGGCCT GAGGGCAGTG AGCCAGGGAG 120
GAGGGAGCAG GACAGCTGGG GGTGCTGGGA AGGAACTGAT GCTCCCATAG TGTCTGAGGC 180
CCTGGCCTCA GAGGCTAGCC CTGGCCCCTG AGCTGCACAT TAATTCTGTT CTGCTGTGGC 240
TTACCCACCA GCCCCCATGC CTGCCTTTTC TCTGTCCCAT TTCCCCCTAC CCCTCCCTGT 300
TGCCATGGTT ACACACACAG GCACTGCCCA GCAACCACCA GGAATATTTC ACTTCGGCCC 360
TGCCCCAAAG CCATAGTAAC CACTCAGCCC ACTTCTGCTT CTGGCTGGGG AATCACAGCC 420
CTCTCTTGCA CAGGCCCCAG TTCGCACCAG TCCCTAGGAC CCCCAGGGAG CCTTCCTGGC 480
TGCCTGCCTA TTGAGGGCCT ATCACCAGCC TGAGGATTTG TGCTGCTGCT GCTGCCGCTG 540
CTGCTAGTAT GCTCCTCTCT TCTGTTCCTA TTCTTCTGAC CTAATTAACG CCCGGTTCTG 600
AAAATCCACC CCTCCCTCTG CCAGACACAA ATTCAGACAC TGTTCTCTTA AAGGTCAAGG 660
TCTAGGGTGG ACAGGGGGAG GTTTCCACTC CAGGCCCAGA GTCTTTCTCT CCTGAGTGTC 720
ACACCCTGCA GGTTGAGTCA AGTTCTGTGC GTGAGGCTGT GCCTGGGGCC AGGAGTCTAG 780
CCATGAGCAA GAACTGGTGA ACCAGACGGG GGCATGTGAG CTGAGGCATG GGCTGGGTTG 840
GGGGAGGACA GGAGAGGCCT GACCTCTCCT GGTGAGATGA GTTAGGGATG GTGCTGTAAG 900
AGGGTGGTCC TGAATGGGGT TGTGAGGAGG TAGAAGGTGT CCAGGTTGAT AGAGGGAACT 960
GCAGCATGAC CGAAGATGGG CCATGGTGAC TGTAGGGACC AGCAAGGGGT TCCATGTCAC 1020
TGGAGAGAAG CCCGCCAGTT AGGCTGCCCC AGAAAGGAGT TTAGATTTTA TCCTGATGGC 1080
CATAGTGATG GCTCGCAGCC CACTATCCCC TGAACAAGAT TGGTCTGCAC AGACAGGCAG 1140
GAGGGTCCCC AGACCCTGGA TGTGCCCAGC CAAGCTTCTT CCCACCCCTG CAGACTGCCT 1200
GGCTCCACCC GCTCCCATCA TAACCTCTTG CTTCCACCAG AATTCCAGGT CAGCCTCCAC 1260
TCGGGGATGT GCATCCTATA ATGCTGCTCC TTCCTGTTCT CCCCATGGGC AGGGCCTCTG 1320
TGCCCCCGTC CTCTCACACC CGAGCCACTC TTGCCTGTTG GAGGCCGCCC CTGTGGGTCC 1380
CCACCCTGGG TGGCCAGAGC TGGGGAGCTG CTGGAGGTGG TGGAGTGGGT CAGTACATCG 1440
CCGGGGACAG AACGAGGGCT GTATTCCTAG TTGGCTCAGG GGACTAGCTC CTGCCAACCC 1500
TCTCCCTAGA ATTTCTTCTC TCTTCCTGTT GGTGGCTGTG TGGGTGGACT TCACTGGGAA 1560
GGAGGGGGAT TTCTTGGCAC CTTCTTTCTC CACTCCTCTC CTTCAACCCT TTGGAGCTCC 1620
TGAGTGGCTC CTGTTCCACA GGCTGACTCC AGAGCTCAGC CTTGCCGGGA TTTCCGGGCA 1680
TCCCGGCACC CTCTCCTGGG CCATCTAAGT CCATGGGGGC ATGGGCAGCA CTCACCAACT 1740
GTGGCAACAG GGCAGCCATC AGAACCCCTG GCCACCAGTC TCTCAGTGAC TGAGCTGTCC 1800
CCCAGGGTGA GTCACTTCCT TGGGTCTTGG AGGTGTTTTG GCTTCCAGAG GCTTCTGGGA 1860
GGACTCCCTC CAGCCCTGCG CTGCAGGACA CACCCAGAGC CTGTGGTCTG GAGGCCTCAG 1920
GGGCTTGGGC TTCTGCCTCC AGCGCCTCAC CTGGAGGAGG GGAGAGCAGT CCTGCCCAAG 1980
GGAAGCTGTG AGGCCCACTT GCTGCATAGG AGGGATGGGG TAGCTCTGAT GAGGGAGATC 2040
TGGGTTTTTA GGGCTGGCAG CTCCTTTTTA TTCGGTTAGG AAGGCTGAGT CCTTGGTCTT 2100
GAGGTCCTGT GTATGGAAGC AGAGGAGGGC AAGTACTATT GTACAGAAGG AGGCTCAGAC 2160
AGAGGGAGGG AGATGCAGGA GAGAGCCCCA TTTGGCAGAG GGGAATGAGC AGGAGAAGGG 2220
AGGATGCTGG GGGCGGCCCC CAGCAGCATC TGCCCAGAAC ACAGCTCTGC CCAGCTCCCG 2280
CACAGCCCTT GGAGTGGGGG TGGATATGTT ACCATTTCTG GCCCCAGAGT GTCCTCTGCC 2340
TAAGTCCCTG CCCTGTGGCT GCTTGGAGGC CCCCATGACT CCTGCAGCTG AGGAGCTTCT 2400
CCCTTTCCAC CTTTTGCCCC CAGCCTGCGT GTTGCCCCCA GGGTATAGAG GTGGGCAGAG 2460
GGGTGGGACT ATCTGCACAT ACCAAAGAAC ACAAGAGTCC CACATCCTTG ATGGGGAGCT 2520
TCTGGCTTGG TGATGAGGAG CTCCCCTCTT GGAATTAGAC AGAATTTCCC GCTCATACAG 2580
CACCTTTCCC TCTCCTACCG CCACCCCCAG CAGCCATCTG GCAACTCTGT GAGCTACTGA 2640
AATCCTCGGC GCTGGACGCC AAGAGCAGAG TTCTTGAGTG TGGGGAAGCT CTCCCTGGGG 2700
AGGGACGGAG GAGAGTTTCC ATGGTTGGAA GGAGCCAGGA GAGGGTCCGG GCTGGACACA 2760
GAGAGGAAGG GAGGGGGGGG CTCTGGGAAT GTCGTTGTCA AAGCTACTTG AGAGGCTGAA 2820
GAGGAAGAGA AGAGGGCACT GGGGGCCACA GCCCAACCTC CCCACCAAGA GTCAAGCAGC 2880
AGAGCCACCT ACCCAATCCA GGCACTTTCA CATCTTAGCC AAAACTCTTG CTGTAATTGT 2940
GAGAATTGCA AACACACCAG GGACTGTTCC ATAAAACGAC TGGCCTGTGC TCCTCAAAAA 3000
TGCCAGTGTC ATGAGAGAGA AAGGTGGAGG GCCGCTTCCA GATACAGGGA GATTAAAGAG 3060
ACATGGCACC TGAATACAAG GTATGATCCT GGACTGGATC CTGGACAATA ATAGTTATAT 3120
AGAGAGAGGA ACATTGAGGA AGGGTTTTCG GTTATGAGAC TATTCTTGCA ACTTTTCTGT 3180
AGGCTTGAAA TTTTGTAGAA TAACAAATTG AATACCAGAA GCTTGACCCC TCAGAACTGC 3240
TCCCTCACCT AAACTGGGCT AAGGGTGAAG GATTTTCTCT CTTGGAGAGG 3290