EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-14679 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr9:127046880-127049250 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GCM1MA0646.1chr9:127047496-127047507CATGCGGGTGC+6.02
Gata1MA0035.3chr9:127049140-127049151TCCTTATCTGT+6.14
ZNF263MA0528.1chr9:127048546-127048567TCCTCCTTTCCCTTCTCCACA-6.16
ZNF263MA0528.1chr9:127048346-127048367CCCCCCTCCCTGCCCTCCCCC-7.66
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01861chr9:127046506-127049775Aorta
SE_02294chr9:127046497-127049969Astrocytes
SE_03002chr9:127046477-127048332Bladder
SE_03002chr9:127048433-127049834Bladder
SE_04593chr9:127046574-127049467Brain_Anterior_Caudate
SE_06625chr9:127043834-127049648Brain_Hippocampus_Middle
SE_09789chr9:127046591-127050293CD14
SE_23712chr9:127046626-127047227Colon_Crypt_1
SE_23712chr9:127047265-127049868Colon_Crypt_1
SE_24006chr9:127047555-127048089Colon_Crypt_2
SE_24006chr9:127048095-127049763Colon_Crypt_2
SE_26169chr9:127046463-127049845Duodenum_Smooth_Muscle
SE_27460chr9:127046556-127049833Esophagus
SE_29975chr9:127046449-127049606Fetal_Muscle
SE_31765chr9:127046641-127049905Gastric
SE_36996chr9:127041377-127050527HSMMtube
SE_38009chr9:127046644-127050178HUVEC
SE_38868chr9:127046466-127050685IMR90
SE_42506chr9:127043941-127049998Lung
SE_44293chr9:127046454-127050001NHDF-Ad
SE_44809chr9:127043918-127049996NHLF
SE_45648chr9:127040018-127051411Osteoblasts
SE_47283chr9:127041647-127050279Panc1
SE_47557chr9:127046812-127047158Pancreas
SE_49326chr9:127046669-127049494Right_Atrium
SE_50283chr9:127046482-127049944Sigmoid_Colon
SE_51779chr9:127046603-127049889Skeletal_Muscle_Myoblast
SE_52726chr9:127046633-127049907Small_Intestine
SE_54297chr9:127046540-127050009Spleen
SE_60448chr9:127019058-127056389DHL6
SE_63558chr9:127046603-127049955HSMM
SE_65907chr9:127046833-127049972Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9127047214127047982
Enhancer Sequence
GCAGGACTGA GGCGGTCTCT ATGGAGTTGT TCTGACTGCA GCTGGGCCCT GTCCTTCCAC 60
ACCTGCCCCT GCAGGAATTC TCCGGACGCC TGTGGAGGGA AGAATGTGTG TGTCTGGGGT 120
CCAAGACCAC ATGCACCGCC TGGTGGAACT TTCTCTGCTC TTGCATGTCT GGTGGGAGCT 180
TCCCTTAATG ACACAGGATC TGCCGAGATT CATCCCCAAC TCCAGGCTGG CACCAGTGTT 240
CAAGCCCCTG CCTCTGCTGT CTCCCAGGTC TTCAAATTTA CACCACTCTG ACTCTCAGTT 300
TCCCTATCTG CAAAATGAAG GCAGGAATGC CCACCTCATG GGGTGAGCCA GTGGACCCAA 360
ATACGTGGTG CAGTAGGTGC CACGGAGTAG TGGCACGTGA TTTTGTGGCT GTTAGTGTGA 420
GTATTCCTTA CTTTAGAGAG CAGAGGAAAA CACATCAGCA GATTGTTTAA GCCAAAAAAT 480
GTCTGTTGTT TGAAGAATTT CGTTTTGGAA GGCAAGCCCA GGTTTTGGGT CAGAACCGTA 540
TTCCCTCAGG CACGGCACGG TTGAACGTCG AGGCATATTT TACAGGCTTG GTGACCGCTC 600
AAGCCTTTGA GCCCTCCATG CGGGTGCTCT GAGGTCAGAC TTTTCGGGAA GCCCTCACAC 660
AGCTGGTCTG CTTGTCGCGT TGGTAGCACC GTTTCCACAG AGCAGGCTCT GTTTGGCTAT 720
GAATAGATGT TTTTCTCACT CTTTTCTTGG ATGCCTGAAT GGCAGGCTCC CCTCCTGCAG 780
TCTCAGAGGC CGACCTGCAT GTAAAACTCC AAGCGGACAT CAGAGTGGGT TCGTCTGTTC 840
CTGCTTGGAC TTGAGGCTCT CAGCAAGGCT CAAAGAGCTG GGTCGATGGC CACCATGACC 900
CAGGGAGCCT CCCGAGAGTC TCCCAGGCTA TAGTTTCTGA AGGCTACTGA GTGAACTGAA 960
GAAATCAGAG TTCATGGAAG AGGCAGCAGA TCCGAGCAAC AGCCGAGATT GAGGAGGATG 1020
GTTCAGGATC TCCAAACACA GGCCCGCTGG CTCCACTGTG TCCAAGCCGC AGATGCAAAG 1080
CCTGTTAGGA CAGAAAGGAC ACGAGATAGC AGCCAGGGCC GGCCGCAGGC AGGAGGGCCG 1140
GGCCACCAGC AGTTAGGAGT GTGGGTTCTG GAGCCACACA ACCGGGGTTC AGATCCCAGT 1200
TTTCCCACCT CTATTGGGCA GCATACTGTA AGCCTCAGTT TTCCCCTTCT GTAAAACGGA 1260
GATAATAATT TACCTGTCTC ACAAGGCTGT TATGAGGATT AAAGTAAGTT AACATCACTC 1320
AAGTGCATAG AACGATGCTG GGTACATACT AAATAAATAC AGATAAACTG AGGCCCAGAG 1380
AGGGCAAGGG ACTTCGCTGT GGTCACTCAG CAAGTCATTG GGGCAGCCAA GGCTGAAACT 1440
CATGACTCCT AGTCTCGTGA ACGGTTCCCC CCTCCCTGCC CTCCCCCGCA GTCAGACTTT 1500
TTAAACACTG CCTTTTGCAG AGGAAATCGC GTGACCCTTC AGCCCACAAG AATTCCGACT 1560
GCACAGAATG TCTGAAACCT CTTCGGGCTG GCTGGGGGCC TTGTTGCAAT TCTATTCAGC 1620
TGTTAGTTCT TTTTTTCCCC TCTCTTTCTT TTAAAGCTCT ATAGGATCCT CCTTTCCCTT 1680
CTCCACAAAT AGAAAAATTA ACCTCTTGAC AAAGGAGTTG GAAGACTTGA GTCCCTGCTG 1740
TGTGTCCCGG AACCAATCCC CCAGCCTCAG GTTCCCCGGC TGTGAAATGA GAAGGTGTCC 1800
TCTGTTGACA GGGAGGTGGC CCCACCTGCC AGTCTGTGAT TGCCACAGAG ACAAGCCAGC 1860
CAAGAAGTGC CACCCTGGAC GAAGGTCGGG TGAGTGCTGA TTAAACAAAA TCTGGTGACG 1920
CATCCTTCTA AGAAGCGAGG CGAAACCCAC CAGAGATGCT GCGTGCTTCT GCCCACCTCC 1980
TCGTGTCAAA GGTGATTTGA GTCATCAGCC TGGCCTGCAC TTTTCTCGCT CTCCTGTTTC 2040
CTTGCAGTGC TCCTGGGCTC CTGAGCCACT CGGGGCTGAG GCCCGGGGGC CAGTTGTGTC 2100
CCATCTGCAG GCCCCAGGGC ATTAGACCTG AGGGGCCTGG TCACCTTCTG ATTTCTGCTG 2160
GGCGCCCCAG CCATGAGCTC CAGAGGCTGC CAGCCTAGGG TGTGAGTCTG TCTCCGAAGC 2220
TGCTGACATG AGTAGGGACT TCCCCTCTCT GAGCTTTAGT TCCTTATCTG TGAAATGGGT 2280
GCATGAGCCC TGCCTGGCAG GGTGAGATGA GGTACACAAG CCCTATCCTA CTTCACTCCC 2340
CTCTTCCTTC CTGCCCGAAA GGCCCTGGCT 2370