Variant report

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:74915702..74917024-chr11:74959078..74959858,3	K562	blood:
2	chr11:74855150..74856113-chr11:74915822..74916648,7	MCF-7	breast:
3	chr11:74640541..74641099-chr11:74915722..74916622,2	MCF-7	breast:
4	chr11:74854818..74856886-chr11:74915338..74916882,2	K562	blood:
5	chr11:74892413..74894687-chr11:74914535..74916760,2	K562	blood:
6	chr11:74733606..74734570-chr11:74915675..74916673,7	MCF-7	breast:
7	chr11:74733674..74734604-chr11:74915406..74916752,8	K562	blood:
8	chr11:74869678..74870459-chr11:74915424..74916683,3	MCF-7	breast:
9	chr11:74910975..74912649-chr11:74914593..74917010,2	K562	blood:
10	chr11:74640507..74641429-chr11:74915550..74916662,6	K562	blood:
11	chr11:74854240..74856798-chr11:74915145..74916958,23	MCF-7	breast:
12	chr11:74850929..74852986-chr11:74916077..74917592,2	MCF-7	breast:
13	chr11:74851279..74852245-chr11:74915585..74916634,10	MCF-7	breast:
14	chr11:74915763..74916910-chr11:74959359..74960694,5	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARRB1-1	chr11:74915055-74917254	NONHSAT023082
2	lnc-NEU3-3	chr11:74914426-74917299	NONHSAT023081

No data

Variant related genes	Relation type
ENSG00000255395	Chromatin interaction

rs_ID	r²[population]
rs12721494	0.84[EUR][1000 genomes]
rs17133809	0.93[ASN][1000 genomes]
rs17133815	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17133831	0.82[EUR][1000 genomes]
rs17133844	0.89[EUR][1000 genomes]
rs17133848	0.89[EUR][1000 genomes]
rs17133858	1.00[EUR][1000 genomes]
rs1801906	0.82[EUR][1000 genomes]
rs2035208	0.82[EUR][1000 genomes]
rs2306167	0.93[ASN][1000 genomes]
rs34827001	0.84[EUR][1000 genomes]
rs41298121	0.82[EUR][1000 genomes]
rs4362167	1.00[EUR][1000 genomes]
rs56738638	0.82[EUR][1000 genomes]
rs56958854	1.00[EUR][1000 genomes]
rs57277559	1.00[EUR][1000 genomes]
rs57279023	0.82[EUR][1000 genomes]
rs57654883	1.00[EUR][1000 genomes]
rs58941788	1.00[ASN][1000 genomes]
rs59390914	1.00[EUR][1000 genomes]
rs59940449	0.87[EUR][1000 genomes]
rs60893479	1.00[EUR][1000 genomes]
rs61265142	1.00[EUR][1000 genomes]
rs61555831	0.93[ASN][1000 genomes]
rs67495709	1.00[EUR][1000 genomes]
rs67947456	1.00[EUR][1000 genomes]
rs7110250	0.87[ASN][1000 genomes]
rs72998556	0.93[ASN][1000 genomes]
rs72998568	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72998587	1.00[EUR][1000 genomes]
rs72998590	1.00[EUR][1000 genomes]
rs72998593	0.96[EUR][1000 genomes]
rs72998594	1.00[EUR][1000 genomes]
rs72998602	1.00[EUR][1000 genomes]
rs73488764	0.82[EUR][1000 genomes]
rs765823	0.93[ASN][1000 genomes]
rs765824	0.93[ASN][1000 genomes]
rs7924924	0.82[EUR][1000 genomes]
rs7927925	1.00[EUR][1000 genomes]
rs7951787	0.82[EUR][1000 genomes]

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74907800-74918000	Weak transcription	Right Atrium	heart
2	chr11:74911400-74919800	Weak transcription	Spleen	Spleen
3	chr11:74912000-74916800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr11:74913800-74918000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr11:74914000-74916800	Enhancers	Liver	Liver
6	chr11:74914200-74916800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr11:74914200-74917200	Genic enhancers	Fetal Intestine Small	intestine
8	chr11:74914400-74917200	Enhancers	Fetal Intestine Large	intestine
9	chr11:74915400-74916400	Enhancers	Fetal Muscle Leg	muscle
10	chr11:74915400-74916400	Bivalent Enhancer	Placenta	Placenta
11	chr11:74915800-74919600	Weak transcription	Lung	lung
12	chr11:74916000-74916400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
13	chr11:74916000-74918600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:74916000-74919600	Weak transcription	Pancreas	Pancrea
15	chr11:74916000-74920800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:74916200-74916800	Enhancers	HepG2	liver

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