EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-08181 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr2:43420510-43423450 
Target genes
Number: 2             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12614953chr243421461hg19
TF binding sites/motifs
Number: 35             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:43422794-43422812CTTTCCTTCCTTCCTTCC-10.53
EWSR1-FLI1MA0149.1chr2:43422798-43422816CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422802-43422820CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422806-43422824CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422810-43422828CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422814-43422832CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422818-43422836CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422822-43422840CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422826-43422844CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422830-43422848CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422834-43422852CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:43422846-43422864CCTTCCTTCTTTCTTTCT-6.56
EWSR1-FLI1MA0149.1chr2:43422786-43422804CTTTCTTTCTTTCCTTCC-6.95
EWSR1-FLI1MA0149.1chr2:43422842-43422860CCTTCCTTCCTTCTTTCT-7.85
EWSR1-FLI1MA0149.1chr2:43422790-43422808CTTTCTTTCCTTCCTTCC-8.46
EWSR1-FLI1MA0149.1chr2:43422838-43422856CCTTCCTTCCTTCCTTCT-9.09
Gata4MA0482.1chr2:43421880-43421891TCTTATCTCCC+6.62
Gfi1bMA0483.1chr2:43423338-43423349AAATCTCAGCA+6.32
NKX2-5MA0063.2chr2:43423250-43423260CTCAAGTGGT-6.02
PAX6MA0069.1chr2:43421205-43421219CCCTCATGCGTGAA-6.06
RARAMA0729.1chr2:43420740-43420758CACTGACCTGCTGACCTT-6.26
TCF7L2MA0523.1chr2:43422153-43422167GTCCTTTGAAGTTT-6.1
ZNF263MA0528.1chr2:43422786-43422807CTTTCTTTCTTTCCTTCCTTC-6.02
ZNF263MA0528.1chr2:43422790-43422811CTTTCTTTCCTTCCTTCCTTC-6.03
ZNF263MA0528.1chr2:43422794-43422815CTTTCCTTCCTTCCTTCCTTC-6.48
ZNF263MA0528.1chr2:43422798-43422819CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422802-43422823CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422806-43422827CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422810-43422831CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422814-43422835CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422818-43422839CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422822-43422843CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422826-43422847CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422830-43422851CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr2:43422834-43422855CCTTCCTTCCTTCCTTCCTTC-6.94
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_03102chr2:43421033-43422155Bladder
SE_11879chr2:43418911-43423261CD3
SE_13409chr2:43420281-43422935CD34_Primary_RO01536
SE_14384chr2:43419736-43423391CD4_Memory_Primary_7pool
SE_16107chr2:43418889-43423186CD4_Naive_Primary_7pool
SE_16950chr2:43419718-43423194CD4p_CD225int_CD127p_Tmem
SE_17323chr2:43418298-43424856CD4p_CD25-_CD45RAp_Naive
SE_17875chr2:43418720-43423486CD4p_CD25-_CD45ROp_Memory
SE_18565chr2:43418586-43425101CD4p_CD25-_Il17-_PMAstim_Th
SE_19552chr2:43419045-43424825CD4p_CD25-_Il17p_PMAstim_Th17
SE_20901chr2:43419730-43423348CD8_Memory_7pool
SE_22349chr2:43418758-43425198CD8_primiary
SE_23059chr2:43418495-43422765Colon_Crypt_1
SE_23724chr2:43419841-43422740Colon_Crypt_2
SE_24685chr2:43419715-43422905Colon_Crypt_3
SE_25333chr2:43419730-43423364DND41
SE_26374chr2:43419705-43422902Duodenum_Smooth_Muscle
SE_26557chr2:43421228-43422781Esophagus
SE_27617chr2:43418343-43423099Fetal_Intestine
SE_28536chr2:43418392-43423198Fetal_Intestine_Large
SE_30898chr2:43419713-43423304Fetal_Thymus
SE_31392chr2:43419752-43422761Gastric
SE_34919chr2:43422110-43423362HeLa
SE_40066chr2:43420058-43423419K562
SE_42201chr2:43419809-43422274Lung
SE_49954chr2:43419904-43422270RPMI-8402
SE_49954chr2:43422272-43422938RPMI-8402
SE_50052chr2:43418452-43423001Sigmoid_Colon
SE_52337chr2:43418468-43423283Small_Intestine
SE_53288chr2:43420099-43422793Spleen
SE_58412chr2:43352450-43425007Ly1
SE_61450chr2:43354337-43468354Toledo
SE_62203chr2:43354169-43468733Tonsil
SE_65350chr2:43419451-43422721Pancreatic_islets
SE_66787chr2:43420870-43422147Jurkat
SE_66787chr2:43422197-43422944Jurkat
SE_68698chr2:43421113-43422308H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr24342122943421631
chr24342200543422472
Number: 1             
IDChromosomeStartEnd
GH02I043190chr24341729043424879
Enhancer Sequence
GTGGGTGGCT GACTACTCTG AGTTTGTGGG TGATTCATGT GTACCCTCGC GACAGGCTGT 60
GTTCAGATAG TCTGCTTATG TGCTTGAATT CAAGGACACA AACATCCCTA GGTGCAAGCT 120
TGCACGCACA GTCCTCCCTA CACCTCCACA CGCAACTCCT AATCATCCCT CAGGATCCTC 180
TCCCCGCCCT GCTTCAGCCT TAAGGCCTGC TCTGACCCTC CAGCCCATCC CACTGACCTG 240
CTGACCTTCA TCCCAGACAC TGCTGGGTTC AGCCCTGGAG CCTGGTCACT CTTGCTCCCT 300
GAGGGTGAGG TTGACTCCTT TTTAAATTAC CCCTAAAGCC CCACTTAGGG AGACACAGCC 360
TTATCAATCA ACACTCCTTG AATGAATTAA AACAAACTCC AAGGAAAGGA ACTGCATTTG 420
GGTGGATGGA AACAAGAGCT CTCAAGCTGT TTTCTTTCCT CTTTACCCTT TGCTCTCTGT 480
CTCTTCCCAT CTGTACTTTC TCTAACTTGT TTGCTAACTC AATCGTCAGC TTAGAAAGTA 540
CTTCCTTGTA TACCCTCCTC TCATTCAAAT CTCATGACAA TCCTCCAAGA CACGAATAAT 600
TATCCTCATT GCACAGATGA GGAAACTGAG GTTCAGGGAG GCTACGTGAG TTGCCCAAGG 660
TCACACAGCC TGGAAGGAGT GGGTAGGGAC TAGAACCCTC ATGCGTGAAT GGACACCACC 720
TCCCACCACT CCCCACCAGT AAGTAGAGGG TGGAGGGTAA AGGGCGATCC AGGGGCTCGG 780
AGAGGATTGG CCTCTTCAAG CCCTCTCCAT GGCCCAAGGT CACCGTGGGA GGGAGATGCA 840
CCTGGCCCCC AGGGCCAGGG GTTACCCCAC TCGGCCAGCA ATGGGAGAGG CCATGAGATC 900
TGTGGACATT GTTCCTGGGC CTGTGGTTAC TGATTTGACA ACAGCCCTGT TCCTCCCCAG 960
CCAGCCAGGG AGTTAATGAT TAAGGAGGAG ATTAAATATT AACCACCTGT GGGGCCACGG 1020
CGTAATGTCT CCATCTGCAC CTGAGCCTAC CTAAAAATCC CTCCCACCTG CCGTGGGCCA 1080
GCCCCACACA GGGCCTCTAA GCCCCTTGCT TAGGGATACC ACTTCCCCAT GCCCCCATCC 1140
TGCCCTGGCC CTGGCCCTGG CCCGTGTCCA CCCCATCTCA CTCTCTCATA CCCACAGCAC 1200
AGACCCAAGG ACTCTTCCTG TAGCTTGGAA GCTGCAAGCT ACACCACTGT AGGCACTCCT 1260
GGTGGGCCTT CTGGAGGAGA GGACCTGCCT GAACCCAGCT ACTCCTGGGG CTTGGAGAGT 1320
CCGCAGGTTA CATTCCTACC TGTGACCTCG TTTATCAGTG CTCTTATCGC TCTTATCTCC 1380
CAAGTCGTTC CTCCTAAAGA CCCCTCTGAA TCTACACATC CCAGGCCCCA ACACCCTGGG 1440
CTACAGCAAC TCCCCAACAC GCCATTCTCT TCTTTCTTCT AGCAGTTAGA ATCTGGGTGT 1500
GTTCTGCCTC CAGGAAGCCT CTCATATTAA CCTGGGCTAA GGTCTCTGCG GGCCTCTGCT 1560
CCCCAGCTTC CCTTAGGCCG GGGTGATTCA GGCTGGCATT GGCTGCTGCA CGGCTGCAGG 1620
AAACCAGCTG CATCTGTTGG AAGGTCCTTT GAAGTTTAAG TGCACAGCCT CCGAGCGCTG 1680
GGGGCGGGGA CTGCTCTATC TCACCTAAGC CTAGGGCCTG CCCCTGGGTG AAGCCATGGT 1740
CACCCTCCCC ACAGCAGGAA CCACAGGCAG TATGACACAG GGTTCACCTG CGTCTTTTTC 1800
TATAAATATA GAAAAATGGA ATTATTTATT CAAATAATAA CTCTATTGAT ATGCTCTCAT 1860
TCCTGTTTGT GGGGAAGCCC CAGATGACTG TGTGGGTAAG TTACTATGGT ACGTAAGCCC 1920
CACCGTAGCC TGGGCCTGCA CTGCTCTCTC TGCATGTCAG TGAACTGCAT TGACACTGCA 1980
GGCCTAGTGA CAGGCAATGT CATCCCCATT TTACAGATGG CGAAACTGAG GCTGGGTGAA 2040
ATTAAAGGAC TTGGCCACGC TCAAACAGAC AGGAAATGGC AGAAGCTGGC CTGCCTGGTG 2100
CAAAAGCCAT ACAAAACTGA AAAGGACCTA ACACCGTTCT TGCCACAGCT GTCTAGGCCC 2160
CAAGCTCAGC TTCTTTTCAG CCACAGTTCC CAACCATGTG TGGCTTGCTT GCTTTTCTTT 2220
CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT 2280
CTTTCTTTCC TTCCTTCCTT CCTTCCTTCC TTCCTTCCTT CCTTCCTTCC TTCCTTCCTT 2340
CCTTCTTTCT TTCTTTCTTT CTTTCTTTCT CTCTTTCGAG ATGGAGTCTC ACTCTGTCAC 2400
CCTCTGCCTC TCGGGTTCAA GCCATTCTCC TCCTGGGTTC AAGCCGTTCT CCTGCCTCAG 2460
CCTCCCGTGT AGCTGGGATT ACAGGCACAC ACCACCACTC CTGGCTAATT TTTGTATTTT 2520
TAGTAGAGAC GGGGTTTCAC CATGTTGGCC AGACTGGTCT CAAACTCCTG ACTTCACTCA 2580
AGTGATCCAC CCTCCTCAGG CTTCCAAAGT GCTGGGATTA CCGGTGTGAG GCACCGCGCC 2640
CGGCCTTTTT GTTTGTTTTT TTAAGACATG GTTTTGCTTT GTCACCCAGG CTGGAGTGCA 2700
GTGGTGCGAT CATAACTCAC TGCAGCCTTG ACCTCCTGGG CTCAAGTGGT CTTCCTGCCT 2760
CAGCCTCCGA AATAGCTGGG ACCACAGGTG TGCACCACCA TGCCTGACTA ATTTAAAAAA 2820
ATTTTTTTAA ATCTCAGCAC TTTGGGAGGC CGAGGTGGGT GGATCACGAG GTCAGGAGAT 2880
CGAGACCATC CTGGCTAATG TGGTGAAACC CTGTCTCTAC TAAAAATACA AAAAATTAGC 2940