EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-22002 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr9:127027850-127031150 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12379417chr9127029736hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GabpaMA0062.2chr9:127028731-127028742CCGGAAGTGAC+6.14
MYCNMA0104.4chr9:127030909-127030921GGCCACGTGGTG+6.07
MYCNMA0104.4chr9:127030909-127030921GGCCACGTGGTG-6.07
Nkx3-2MA0122.3chr9:127030559-127030572ATTAAGTGGTTTA-6.92
RUNX1MA0002.2chr9:127029896-127029907TTCTGTGGTTT+6.32
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_01861chr9:127028027-127030811Aorta
SE_02294chr9:127028292-127030548Astrocytes
SE_03002chr9:127027842-127028520Bladder
SE_04593chr9:127028891-127030342Brain_Anterior_Caudate
SE_06625chr9:127028933-127030320Brain_Hippocampus_Middle
SE_09789chr9:127025946-127031287CD14
SE_23712chr9:127027894-127031158Colon_Crypt_1
SE_24006chr9:127027853-127028277Colon_Crypt_2
SE_24006chr9:127028279-127028609Colon_Crypt_2
SE_24006chr9:127028617-127030420Colon_Crypt_2
SE_26169chr9:127028464-127031167Duodenum_Smooth_Muscle
SE_27460chr9:127028546-127029502Esophagus
SE_27460chr9:127029577-127030298Esophagus
SE_29975chr9:127028907-127030325Fetal_Muscle
SE_31765chr9:127027836-127031189Gastric
SE_36996chr9:127027502-127031245HSMMtube
SE_38009chr9:127027450-127031685HUVEC
SE_38868chr9:127028106-127031763IMR90
SE_42506chr9:127027674-127031138Lung
SE_44293chr9:127028727-127031058NHDF-Ad
SE_44809chr9:127028276-127028828NHLF
SE_44809chr9:127029011-127029548NHLF
SE_45648chr9:127018281-127031420Osteoblasts
SE_47283chr9:127027822-127030793Panc1
SE_47557chr9:127029471-127030049Pancreas
SE_50283chr9:127027697-127031101Sigmoid_Colon
SE_51779chr9:127028340-127030620Skeletal_Muscle_Myoblast
SE_52726chr9:127027715-127030348Small_Intestine
SE_54297chr9:127028449-127030673Spleen
SE_59258chr9:127016097-127031007Ly3
SE_60141chr9:127018983-127030974Ly4
SE_60448chr9:127019058-127056389DHL6
SE_63558chr9:127028209-127030812HSMM
SE_65907chr9:127028092-127030478Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9127028281127028331
chr9127028725127030267
Enhancer Sequence
TTTTACAGAT GGCGACACTG AGGCCCAGAG AGACATCATG ACCAGCCTCA GGTCCCACAT 60
GCAGCCTGCT GCTCTGTAGC CTAAATCAGA TCACTGTCCC AGCTTTCAGG TCAAGGCTCT 120
GGTTGTGACA CCTGGGCCTG GACTGCGGGT GAAAAGTTTT GATGCAAAAA CACAGACCGT 180
CCATTGTCCT ATGGGCTAAG TGGACTCCCT TCTGCTAACC AGAGATGCTT GTGCTGGCTG 240
GTGTGTGGCA CGTTATCTCA TTCTTTCATG ACGTATGTCC GGATGGAAGT CCTGGGTCAG 300
GCATTGTGCT GGGAGCCCAC ACGAAGACCC TCTAATGGCC CCACCCATTG GCCTCTCACC 360
ACCTGGTGGG GACAGAGGCT GTCACAACCC CTTCTTAGGT GCTCTTGATC AATTTGCAGG 420
TGGCATTTTT TGGGATGTAG TCTCTGGGGA AGTAGGAGAG CTTCCGGCAG TGAGGGGTGT 480
TTGAACCCAC CTGGAGGGAG ACGTGGGGTT TGCCAGAGGG CTGAGAGGGC TGGGGTGAAG 540
GGCAGGTAGA CCCCAAGGTG GAGAGGCAGG TGGGGCCGGT GGGTGAGAGG TGGGGCTGTG 600
GAACTTCCTC CTGCTTCTTT GGCCTTTGCT CCTGTCGGTA GATGGCCTTA CCAGGCACTT 660
ACTGTGGGCC ATGTTCTAAT CTAACCCTTA ACCTGAGGGA ACTCACTTCA TCCTCCCAGT 720
GATGCCGTGA TGTGGGTATC GTTCTGCCCA TTTTATAGAT GAGGAAACAG AGACCCAGAG 780
AGTCCAGGAT CTGTGGTGCT TGACGAGCAT CAGCCTGAGT GCTGTGAGGA CACCCACAGC 840
ATGGGGGTCT GAGCTGAAAA TTGGAGGACA GAGGCTGCCC TCCGGAAGTG ACCAGGATGT 900
GCCCTCAGGA AGTGACCAGC TGCCCAGCTC AGGACCTGTG TGAGGGCCCC CAGGCAGCTG 960
GAAGGAACAG TGTGCACCCA GGTACCATGC CAGGGCCCCT GAGCATCCGT CTTGTCATCG 1020
CATAGTTGTA ACCTGCCTCA CAGACTGAAC ATGCACTCTA GAAGGGGATG GGACTTGGTC 1080
TGTGGACCAC AACAGTGTTC TCCATGGCCA GCATTGTGCC TGACACATAG GAGGAGCTCA 1140
ATTAATATTT GTTGAGTGAA TGGGAAGTTT TAAGTAGGCA CGCGGCCGGA TCCTTGGAGA 1200
ATGTTTATAT GGAGTGAACG AATCTGTTAG CAAACGTTCC TCACTCCCCT CAGTGGGCTG 1260
TGCAGGGCTG TATTGAGCTG AGCTGGCCCT TCCCTGGGAG AAGAGGTTTC TTAGAGAAAT 1320
GCTCATCCTC GAATTATTCC AATGAGGAGG AACCTAAGCC CAGAAGGGCT CTACCTCCCA 1380
GAGTTACAGG CTCTCCTTCC TATGCCCCTT CCCTGCCGAG GCAGCTCCCA CATGTCTGCA 1440
TAGGAGGGCT TTGGGTTGGA ATGGGTCAGT GCTGTGTCTT AAAGCTGCAT TTTCTACCAA 1500
GCACACACTT TGTTTAGAGG GCATATCTTT TGGGGTTGCT TTGAGGAAAG GCTAACCAAG 1560
CCACCTCTGA GCACAGACAT GACTTTTTGG CAAATGAGCA GGACCCCAGA TTACACCCCA 1620
TCTTAGAAAG TAGGAAACCC AGCATTGAAA GAGGAAAGAT TCTGCAGCTG ATGTGGCCTT 1680
GGCGGGCCAC CAGCGTGGGT GCCCAGATGG CAGGATCACT GGGCACCACA TGGCACACAG 1740
AAGAGAGCAA AGGAGAGGGA GTCCGCCCCT GGGCTTGGCA GGTCCGGTCG AGTCCGCCTG 1800
GATTCAGTTA CAACAGGACC TCGAGTGGGC ACGGCGTGCC GGACTGAGTC AGTGTGTGTA 1860
CATTTCCTTT GTTCGTCTCC TCCGGGAATG TAGTGGCCTT TTGTGTGTGT TTTAAATGCC 1920
AGCCTCCTTA CCTAACCCAA GAGGAAATGA GGACTGGGTT TTTGTCTGTG CAGACGCTGG 1980
GACAAGTGTG GGAGCCGCCT GCTCTTGGAG CCAGCCTAGT GGTGACAGCG TGGCATTTGG 2040
AAAACATTCT GTGGTTTTCT CCAAGGGGTG ATGGGCACAC CAGGTGCTGG GCCGCCCCTG 2100
AGCTGGCCAC TGGGACCCTG AAATGAGGAA GCCCTGTGAC CAGGTTTCAT GATGCCATTC 2160
AGCAAGGGAC GGCTGAGCAC CACATGCCTT CTTGGCCCCT GGGGAAACAC ACAGGAATCA 2220
GATGAGGTCC CTGCCCCGTC TTCCTGGGGA AACATGCAGA GAAAATACTT GTACTCTGAG 2280
CTAACACCTT TCACTCGCAC AGACCTTTAT GGTGTTCTGT GTCTTCAGAC ATTGATCACC 2340
TGTAGGTGAG ACACATCATG GCCCCACTTT CCAAACTCCC AAACGGGCTG TGATCTGTAG 2400
AAGTATTTAG TGCCATTCAG GGACAGGAGA GATGGTTTGG AAGATGCTGT CTGCTGTGCG 2460
AAGTCTCTGG ATGCTCAAAT GGCTTATGGG GTGGCATCTT TGAAATTACC CAGTCCTGAA 2520
AATTTCAGGA CATATGGTCA CTGTGATGTG CTAATGTTAG CAATTGAGAT ATTTAATGAC 2580
CCAGAAAAAC CCCTTTTCCT ACCCAGTGCA GGTTACTGGA GAGCCTTTAT TTCTCAGGAG 2640
GAGGGTCTTA CACAGTGTAA TTTGGACCAG CAGATAGGGA GTCATTATCC CTCATTCATT 2700
TATTAGCTAA TTAAGTGGTT TATCTGGTCA CACATTTACT CCTTCAATTG CCATTCATCC 2760
AGCACTGTTT GCTGATGTAC CTGGCCTGGT GCTGGGTACT GGGGGTGGAA TGAAACAGAA 2820
CAAATATGAC TGAGTCCCTA CTGTGTGCCA GCCCATAGGG TGTGCTGTGT GCCACAGGTG 2880
AATGCATTCA CTTCCCAGTG GACATTTAAC AACCACCTAC TGTGTGCAGA CTCATGGAGA 2940
TGCAGAAATG CAAATGGCAC AGTCCGTAGT GGTTTGGACA CTTGTGGTGT TTTGATGGGG 3000
TCTTTAGTCC TGGCTCTCTC TCTGCTTGCT GTGATATACC CAGTCAGCCA CTGTTCACAG 3060
GCCACGTGGT GACGTCCCCA GAATGAACCA GAAACAATCC AGATGCCCCA GGAACCGACG 3120
TGAGAACAAG GCATCCCCTT CACACGTTGT GTCTCAGTTC AGCGTCTTGC CACCACCCAG 3180
CATTTTGAGA CAGAATGTGA GATCGCGTGG TTGGCTAAAT ACATAAATAT TTTATGTCTC 3240
GATATTCTGA AAATGAAGCC CAAATGCACA GAACTGCAGC ACATCAGTGC TATAGATCAT 3300