Variant report

Variant	esv10922
Chromosome Location	chr7:2757395-2759983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:2758216..2760821-chr7:2762447..2764162,2	K562	blood:
2	chr7:2710355..2711188-chr7:2758257..2758996,5	MCF-7	breast:
3	chr7:2756357..2758230-chr7:2913588..2915207,2	K562	blood:
4	chr7:2393560..2395423-chr7:2757362..2759137,2	K562	blood:
5	chr7:2755108..2759929-chr7:2796424..2799629,5	K562	blood:
6	chr7:2695858..2698224-chr7:2755632..2757966,2	K562	blood:
7	chr7:2724386..2733394-chr7:2753206..2761980,25	MCF-7	breast:
8	chr7:2727234..2729043-chr7:2757444..2760192,2	MCF-7	breast:
9	chr7:2756196..2760316-chr7:2775723..2779597,5	K562	blood:
10	chr7:2729178..2731029-chr7:2755632..2757456,2	MCF-7	breast:
11	chr7:2593899..2596439-chr7:2755739..2757666,2	K562	blood:
12	chr7:2758388..2761774-chr7:2912256..2915270,3	K562	blood:
13	chr7:2758129..2761976-chr7:2763173..2766287,3	MCF-7	breast:
14	chr10:112773361..112773861-chr7:2758450..2759306,2	MCF-7	breast:
15	chr7:2757202..2759716-chr7:2762662..2764833,2	K562	blood:
16	chr7:2758294..2760218-chr7:2772871..2774400,2	MCF-7	breast:
17	chr7:2751778..2761552-chr7:2768388..2775125,13	K562	blood:
18	chr7:2756029..2757761-chr7:2771814..2773662,2	MCF-7	breast:
19	chr7:2757306..2759067-chr7:2759260..2762192,2	K562	blood:
20	chr7:2749908..2752648-chr7:2759444..2761951,3	MCF-7	breast:
21	chr7:2755108..2758694-chr7:2796336..2799311,5	K562	blood:
22	chr7:2749256..2751916-chr7:2756659..2758882,3	K562	blood:
23	chr18:33161346..33162077-chr7:2758154..2758655,2	HCT-116	colon:
24	chr7:2650921..2653062-chr7:2755839..2758657,2	MCF-7	breast:
25	chr7:2710494..2711221-chr7:2758292..2759192,2	MCF-7	breast:
26	chr7:2757306..2759067-chr7:2759260..2762192,2	K562	blood:
27	chr7:2739959..2741756-chr7:2757335..2758890,2	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNA12-2	chr7:2757467-2760269	XLOC_006335

No data

Variant related genes	Relation type
ENSG00000106263	chromatin interactions
ENSG00000141429	chromatin interactions
ENSG00000174945	chromatin interactions
ENSG00000106009	chromatin interactions
ENSG00000106266	chromatin interactions

Extended variants
information (count: 183 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:183 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114423206	chr7:2757405-2757406	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs6965989	chr7:2757420-2757421	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs141788396	chr7:2757421-2757422	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs574003071	chr7:2757425-2757426	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs542718371	chr7:2757484-2757485	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs543898871	chr7:2757490-2757491	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs188302527	chr7:2757521-2757522	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs6979597	chr7:2757534-2757535	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs118184905	chr7:2757538-2757539	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs565568456	chr7:2757553-2757554	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs527948319	chr7:2757554-2757555	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs559985494	chr7:2757560-2757561	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs567122116	chr7:2757568-2757569	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs533711688	chr7:2757598-2757599	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs536279781	chr7:2757605-2757606	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs193065680	chr7:2757614-2757615	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs150554846	chr7:2757617-2757618	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs71527404	chr7:2757618-2757619	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs377716268	chr7:2757619-2757620	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs71527405	chr7:2757630-2757631	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185790388	chr7:2757650-2757651	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs554867053	chr7:2757668-2757669	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs77758578	chr7:2757699-2757700	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs189871256	chr7:2757701-2757702	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs113791921	chr7:2757706-2757707	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs530396757	chr7:2757707-2757708	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs556689614	chr7:2757709-2757710	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs576648298	chr7:2757718-2757719	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs547854036	chr7:2757735-2757736	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs545527526	chr7:2757744-2757745	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs139578041	chr7:2757747-2757748	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs150005717	chr7:2757766-2757767	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs182048567	chr7:2757771-2757772	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs561655175	chr7:2757805-2757806	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs79756242	chr7:2757823-2757824	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs185551583	chr7:2757829-2757830	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs569320064	chr7:2757841-2757842	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs532034601	chr7:2757845-2757846	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs798563	chr7:2757867-2757868	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs565506395	chr7:2757883-2757884	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs798562	chr7:2757938-2757939	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs57754714	chr7:2757963-2757964	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs188698708	chr7:2757977-2757978	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs536239909	chr7:2757980-2757981	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs556555277	chr7:2758010-2758011	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs376768282	chr7:2758013-2758014	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs576506744	chr7:2758058-2758059	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs375287908	chr7:2758078-2758079	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs368323787	chr7:2758082-2758083	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs147701146	chr7:2758101-2758102	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Acute myeloid leukemia	19651601	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Cancer	17160897	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17142309	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:2742200-2765600	Weak transcription	HSMM	muscle
2	chr7:2749000-2760800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr7:2749400-2770600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:2749800-2757600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr7:2749800-2758000	Weak transcription	Brain Anterior Caudate	brain
6	chr7:2749800-2759800	Weak transcription	HMEC	breast
7	chr7:2749800-2770800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:2750000-2757400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:2750000-2760400	Weak transcription	Hela-S3	cervix
10	chr7:2750000-2760800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr7:2750000-2762800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:2750000-2765600	Weak transcription	Brain Substantia Nigra	brain
13	chr7:2750000-2767800	Weak transcription	Osteobl	bone
14	chr7:2750000-2768400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr7:2750000-2769000	Weak transcription	NHDF-Ad	bronchial
16	chr7:2750200-2757600	Weak transcription	HepG2	liver
17	chr7:2750200-2757800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:2750200-2765800	Weak transcription	Liver	Liver
19	chr7:2751000-2759000	Enhancers	Fetal Heart	heart
20	chr7:2751000-2764400	Weak transcription	Brain Germinal Matrix	brain
21	chr7:2751200-2768400	Weak transcription	Brain Angular Gyrus	brain
22	chr7:2751800-2757800	Enhancers	Left Ventricle	heart
23	chr7:2752400-2758400	Genic enhancers	Placenta	Placenta
24	chr7:2752400-2796000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:2752800-2757600	Enhancers	Fetal Muscle Trunk	muscle
26	chr7:2753400-2760400	Weak transcription	Aorta	Aorta
27	chr7:2753400-2765800	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr7:2753600-2759200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr7:2753600-2768800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:2753800-2758200	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr7:2753800-2760400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr7:2754000-2757800	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr7:2754000-2758600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr7:2754000-2759400	Enhancers	Primary B cells from cord blood	blood
35	chr7:2754200-2757600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:2754200-2759400	Enhancers	Primary B cells from peripheral blood	blood
37	chr7:2754400-2757400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr7:2754400-2759000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:2754400-2759200	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr7:2754400-2759200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr7:2754600-2758400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr7:2754600-2758800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr7:2754600-2759000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr7:2754600-2759200	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr7:2754600-2766800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr7:2754800-2757400	Enhancers	Dnd41	blood
47	chr7:2754800-2757800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr7:2754800-2758200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:2754800-2758400	Strong transcription	H1 Cell Line	embryonic stem cell
50	chr7:2754800-2760600	Enhancers	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links